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The Future of Academic Publishing: Trends and Predictions

Academic publishing is undergoing a significant transformation, driven by technological advancements, changing attitudes toward knowledge dissemination, and the need for greater transparency in research. As medical writers, it’s crucial to stay informed of these developments to better serve our clients and contribute to the evolving scholarly communication ecosystem. This blog explores emerging trends and predicts future developments in academic publishing, with a focus on their implications for medical writing.

Open Peer Review: Transparency in the Evaluation Process

One of the most notable trends in academic publishing is the move toward open peer review. Traditionally, peer review was typically a closed process, with reviewers remaining anonymous and their comments hidden from public view. However, there’s a growing push for transparency in this crucial step of scholarly publishing.

Open peer review can take various forms, ranging from simply publishing reviewer reports alongside the final article to revealing reviewer identities and allowing public comment on preprints. This shift towards openness aims to address several issues in the current system, including:

  1. Accountability: By making reviewer comments public, there is increased accountability for both reviewers and authors.
  2. Credit for Reviewers: Open peer review allows reviewers to receive recognition for their contributions to the scientific process.
  3. Educational Value: Early career researchers can learn from seeing high-quality peer reviews.
  4. Reducing Bias: Open peer review may help diminish some forms of bias in the review process.

For medical writers, this trend necessitates a deeper understanding of the peer review process and the ability to guide clients through more transparent scholarly communication. We may need to assist authors in preparing responses to reviewer comments that will be publicly visible, requiring a more tactful and constructive approach.

Data Sharing Policies: Enhancing Reproducibility and Transparency

Another significant trend is the implementation of stricter data-sharing policies by journals and funding bodies to promote open data. This push aims to enhance research reproducibility, allow for secondary analyses, and increase overall transparency in scientific research.

Key aspects of this trend include:

  1. Mandatory Data Availability Statements: Many journals now require authors to include a statement on how and where their data can be accessed, fostering data transparency.
  2. Data Repositories: The use of specialized repositories for different types of data (e.g., genomic, imaging, clinical trial data) is becoming more common.
  3. FAIR Principles: There is an increasing emphasis on making data Findable, Accessible, Interoperable, and Reusable, promoting data usability and accessibility.

For medical writers, this trend requires a thorough understanding of data management practices and the ability to guide clients in preparing their data for sharing. We may need to assist in writing clear data availability statements, ensuring proper data anonymization, and navigating the complexities of various data-sharing platforms.

Artificial Intelligence in Publishing: Shaping the Future

Artificial Intelligence (AI) is poised to revolutionize various aspects of academic publishing. While it will not replace human expertise, AI will likely augment and streamline many processes. Some key areas where AI is making inroads include:

  1. Manuscript Screening: AI tools can help editors quickly assess whether submissions meet basic criteria and are within the journal’s scope.
  2. Plagiarism Detection: Advanced AI algorithms can detect not just verbatim copying but also paraphrased content and idea plagiarism.
  3. Reference Checking: AI can verify the accuracy and completeness of citations more efficiently than manual checking.
  4. Language Polishing: AI-powered tools can assist in improving the clarity and grammar of manuscripts, particularly beneficial for non-native English speakers.
  5. Peer Reviewer Matching: AI algorithms can suggest appropriate reviewers based on the manuscript’s content and reviewers’ expertise.

As medical writers, it is essential to stay informed about these AI tools and potentially incorporate them into our workflow. However, it is crucial to maintain a critical eye and not over-rely on AI-generated content or suggestions.

Preprint Servers: Accelerating Scientific Communication

The rise of preprint servers, such as medRxiv for health sciences, is another trend reshaping academic publishing. These servers allow researchers to share their findings rapidly, before the often lengthy peer review process. This trend has several implications:

  1. Faster Dissemination of Research: Crucial in fast-moving fields or during health crises like the COVID-19 pandemic.
  2. Increased Visibility: These can attract collaborators and feedback early in the research process.
  3. Establishing Priority: Researchers can stake their claim to ideas and findings earlier.

However, the proliferation of preprints also raises concerns about the quality of non-peer-reviewed research entering the public domain. As medical writers, we may need to help clients navigate the decision of whether to post preprints and assist in preparing manuscripts that clearly state their preprint status.

Predictions for the Future of Academic Publishing

Looking ahead, several developments are likely to shape the future of academic publishing:

  • Blockchain for Peer Review: Blockchain technology could be used to create a transparent, immutable record of the peer review process, potentially addressing issues of trust and accountability.
  • AI-Assisted Authorship: While AI will not replace human authors, it may play a larger role in literature reviews, generating hypotheses, and even drafting sections of papers.
  • Interactive Papers: Future academic papers may incorporate multimedia elements, live data visualizations, and even virtual reality components to create a more interactive reading experience.
  • Micro-publications: There may be a shift towards publishing smaller units of research, such as individual experiments or observations, rather than waiting to compile a full paper.
  • Continuous Publishing: Some journals may abandon the issue and volumes-based model, instead publish articles on a rolling basis as soon as they are ready.
  • Alternative Metrics: Traditional impact factors may be supplemented or replaced by more diverse metrics that capture societal impact, policy influence, and public engagement.
  • Open Access Dominance: The trend towards open access is likely to continue, potentially becoming the dominant model for academic publishing, with more journals making their content freely available online.

Peer Review Evolution: These may become more collaborative, with reviewers and authors working together to improve papers through multiple rounds of feedback.

Implications for Medical Writers

These trends and predictions have significant implications for medical writers:

  1. Expanded Skill Set: We will need to develop new skills, such as data management, AI tool utilization, and multimedia content creation.
  2. Ethical Considerations: As AI becomes more prevalent in writing and publishing, we willneed to navigate complex ethical issues around authorship and originality.
  3. Adaptability: The publishing landscape is likely to remain in flux, requiring us to stay adaptable and continuously update our knowledge and practices.
  4. Client Education: We will play an important role in educating clients about new publishing models, data-sharing requirements, and the evolving peer review process.
  5. Quality Assurance: With the rise of preprints and AI-assisted writing, our role in ensuring the quality and accuracy of scientific communication will become even more crucial.
  6. Interdisciplinary Collaboration: As research becomes more complex and data-intensive, we may need to collaborate more closely with data scientists, statisticians, and other specialists.

The future of academic publishing is exciting and challenging, with trends towards greater openness, transparency, and technological integration. As medical writers, we are uniquely positioned to help navigate this changing landscape. By staying informed about these trends and developing new skills, we can continue to play a vital role in ensuring effective and accurate scientific communication.

The key to thriving in this evolving environment will be our ability to adapt, embrace new technologies while maintaining a critical perspective and continue to prioritize the clear and accurate communication of scientific ideas. As we move forward, our expertise in crafting compelling narratives and translating complex scientific concepts will remain invaluable, even as the medium and methods of publishing continue to evolve.

Turacoz Healthcare Solutions stands at the forefront of academic publishing, offering comprehensive medical writing services that cater to the needs of researchers, clinicians, and academicians. Our team is adept at navigating the complexities of modern publishing, from open peer review to AI integration and data sharing. Partnering with Turacoz, you gain access to a wealth of knowledge and experience to help you publish confidently and clearly. Visit www.turacoz.com or contact us at [email protected] to learn more about how we can support your academic publishing journey.

Integral Drug-Device Combinations: Minor Variations to the Device (or Device Part)

The European Medicines Agency (EMA) has released a question-and-answer guidance on the implementation of Regulations (EU) 2017/745 and (EU) 2017/746 concerning medical devices and in vitro diagnostic medical devices. This document offers practical insights into implementing these regulations for combination products comprising both medicinal products (or substances) and medical devices. Such products fall under either the pharmaceutical or medical device framework, depending on their primary mode of action.

The guidance document covers regulatory and procedural guidance for:

  1. Integral drug-device combinations (medical devices that form an integral product with a medicine, such as pre-filled syringes) and their lifecycle management.
  2. Medicinal products that include a medical device in their packaging (referred to as co-packaged) and how these should be labeled.
  3. The consultation procedure for medical devices with an ancillary medicinal substance (a substance that supports the proper functioning of the device).
  4. The consultation procedure for companion diagnostics, diagnostic tests that are essential for the correct use of a specific medicine.

How to Submit Minor Variations to the Device (or Device Part):

  1. As for any other changes, the market authorization holder (MAH) should determine whether there is a potential impact on the delivery, quality, safety, and/or efficacy of the integral Drug-Device Combination (iDDC).
  1. If the MAH determines that the change impacts the registered information, or if the change does not impact the registered information but the MAH concludes that there is an impact on the delivery, quality, safety, and/or efficacy of the iDDC, a variation application should be submitted.

The MAH of the integral combination has the overall responsibility to ensure that the device used in the integral combination is supported by an up-to-date notified body (NB) opinion.

Minor changes to the device (or device part) that do not impact the safety or performance of the device (part), or the intended use of the device but still require an update of the registered information in the marketing authorization application (MAA), should be submitted with the corresponding variation application according to the variation guideline. The MAH should assess and provide justification whether the change has no significant impact on the device to justify the absence of a NB opinion. Otherwise, proof of compliance with the Medical Device Regulation (MDR) should be provided. An assessment of the proposed change will be performed case by case upon submission. In cases where the need for a variation and/or the category of the change is unclear, it is recommended to consult the national competent authority for medicinal products that issued the Market Authorization.

Some Examples:

  1. Change in Qualitative and/or Quantitative Composition of a Device (Part)

The replacement of a material (change in qualitative and/or quantitative composition) of a device (part) by an equivalent one for a medical device (part) that is not in contact with the medicinal product but requires an update of the registered information can be submitted as type IA notification under B.II.e.6 – change in any part of the (primary) packaging material not in contact with the finished product formulation (such as the color of flip-off caps, color code rings on ampoules, change of needle shield (different plastic used)), as long as all conditions stated in the Variations guideline are met.

The replacement of a material (change in qualitative or quantitative composition) by an equivalent one for a medical device (part) in contact with the medicinal product should be submitted under the B.IV.1 category of variation classification.

If the change in composition also includes a change in manufacturer, both should be submitted in a single variation under the B.IV.1.z category of variation classification, type IB, or type II depending on the criticality.

  1. Change in the Sterilization Method for a Device (Part)

Changes to the sterilization method for the device part of an iDDC with no change in the sterilization site should be submitted under the B.II.b.3 category of variation classification.

If there is a change in manufacturer, the addition of a new sterilization site with the corresponding sterilization method should be submitted under the B.II.b.1 category of variation classification.

Of note, in case of several changes to the existing device resulting in the addition or replacement of a new syringe (e.g., change not limited to the supplier of some device parts of the existing syringe but other changes are introduced as well such as an alternative syringe with changes to the design and materials of the existing device parts), both the change in composition including the change in manufacturer should be submitted in a single variation under the B.IV.1.z category of variation classification, type IB, or type II depending on the criticality.

  1. Change in Dimensions to a Device (Part):

Changes in dimensions to a device (part) not in contact with the medicinal product (such as finger grip, plunger rod) that do not impact the functionality or performance of the device but still require an update of the registered information can be submitted as a type IA notification under B.II.e.6 category, as long as all conditions stated in the European Commission variation classification guideline are met.

Changes in dimensions to a device (part) in contact with the medicinal product (such as needle, syringe barrel, plunger) that require an update of the registered information should be submitted as a type IB or type II variation under the B.IV.1 category of variation classification, depending on the criticality of the change.

  1. Change in Suppliers of a Device (Part):

Suppliers of the device (part) for iDDC should be stated in section 3.2.P.7 according to the Quality Working Party (QWP) – Biological Working Party (BWP) guideline on medicinal products used with a medical device.

A variation under category B.II.e.7 of variation classification – change in supplier of packaging components or devices of the guidance for applicants for the preparation of the ‘precise scope’ section of the variation application form (EMA/220707/2017), should be submitted to add/delete a supplier of a medical device (part).

In case of addition or replacement of the supplier of the device (or device part), if the risk assessment performed by the MAH has concluded that the change is non-significant and there are no other changes to the device beyond the change in suppliers, a statement can be included in the submission to justify the absence of an NB opinion / EU certificate/ EU declaration of conformity.

If the device manufacturer is also performing sterilization and the device (part) is supplied as sterile ready-to-use, the change should be submitted under the B.II.b.1 category of variation classification in line with submitting the transfer of test methods for testing of biological medicinal products to a new or already authorized testing site.

For more information, please refer to the official guidance provided by the European Commission. You can access the document at the below link:

Questions and answers on implementation of the medical devices and in vitro diagnostic medical devices Regulations ((EU) 2017/745 and (EU) 2017/746): [https://www.ema.europa.eu/en/documents/regulatory-procedural-guideline/questions-answers-implementation-medical-devices-vitro-diagnostic-medical-devices-regulations-eu-2017-745-eu-2017-746_en.pdf]

Narrative Writing in Clinical Research: Guidelines for a Medical Writer

Medical writing is a specialized discipline within the clinical research domain, focused on preparing scientific documents. These documents must adhere strictly to guidelines regarding their structure, content, and format. Narrative writing is a crucial component of medical writing services, particularly in crafting patient narratives to summarize identified adverse events (AEs) and establish causal relationships with investigational drugs. These narratives, typically one to four pages long, are submitted alongside the clinical study report (CSR), with large trials potentially generating hundreds of narratives. Sponsors often outsource narrative writing activities to effectively manage the demands of cost, time, and quality in project management. We at Turacoz Healthcare Solutions have been in this business for a decade catering to diverse clientele.

This blog aims to guide medical writers in understanding the narrative writing process (NWP), regulatory standards, challenges, mitigation strategies, and emerging trends in narrative automation. Patient narratives summarize AEs observed in clinical trial patients, including criteria such as death, serious AEs (SAEs), events of special interest, AEs leading to drug discontinuation, and adjudication events. Structured with clarity and precision, they provide medical and scientific context, typically following a logical flow:

  • Description of the event’s clinical course, including timing concerning drug administration.
  • Details on the nature, intensity, and outcome of the event.
  • Relevant laboratory findings and administered treatments.
  • Actions taken regarding the study drug.
  • Postmortem findings (if applicable) and assessments of causality by the investigator and sponsor if necessary.

Moreover, patient identifiers, demographics, medical history, and concurrent medications should also be included to provide comprehensive context.

Types of Narratives

  1. Descriptive Narratives: Focused on providing a detailed account of the research process, from study design and methodology to data collection and analysis. Descriptive narratives aim to paint a comprehensive picture of the research endeavor, guiding readers through each phase with clarity and precision.
  2. Analytical Narratives: These delve deeper into the interpretation and implications of research findings. They analyze the data within the context of existing literature, identify patterns or trends, and offer insights that contribute to advancing scientific knowledge or update clinical practice.
  3. Persuasive Narratives: They aim to convince readers of the significance and validity of the research findings. Leveraging compelling storytelling techniques, persuasive arguments, and evidence-based reasoning to sway the reader’s opinion or influence decision-making processes.

Process of Narrative writing

Narrative writing is a complex process involving various departments that begins with template finalization which is a crucial step in the NWP as it avoids subjectivity.

  • Research and Planning: Begin by conducting thorough research on the topic, familiarizing yourself with existing literature, and identifying key research questions and objectives. Plan the narrative structure, outlining the main sections and their respective content.
  • Drafting: Write the initial draft of the narrative, focusing on clarity, coherence, and engagement. Pay attention to storytelling elements such as narrative arc, character development (e.g., study participants), and thematic coherence.
  • Revision and Editing: Review the draft critically, refining the narrative for clarity, accuracy, and conciseness. Eliminate unnecessary details, strengthen the argumentation, and ensure consistency in style and tone. Seek feedback from peers or subject matter experts to enhance the quality of the narrative.
  • Finalization: Incorporate feedback and make final revisions to the narrative. Ensure adherence to formatting guidelines and standards for scientific writing. Proofread the document meticulously to correct any errors in grammar, punctuation, or spelling.

Challenges in NWP

Balancing Objectivity and Subjectivity: Striking the right balance between objective reporting of facts and subjective interpretation of findings can be challenging. Avoiding bias while presenting research results objectively requires careful attention to language and tone.

Complexity of Scientific Concepts: Communicating complex scientific concepts in a clear and accessible manner poses a significant challenge. Medical writers must employ effective strategies such as analogy, visualization, and plain language to enhance understanding among diverse audiences.

Time Constraints: Meeting tight deadlines while ensuring quality and accuracy can be daunting. Effective time management, prioritization, and collaboration with team members are essential to overcoming this challenge.

Effective Ways to Execute Narrative Writing Process

  • Collaborative Approach: Foster collaboration and communication among multidisciplinary team members, including researchers, clinicians, statisticians, and editors. Leverage each team member’s expertise to enrich the narrative and ensure its accuracy and relevance.
  • Iterative Writing Process: Embrace an iterative writing process that involves multiple rounds of drafting, revision, and feedback. This iterative approach allows for continuous improvement and refinement of the narrative until it achieves optimal clarity and impact.
  • Utilization of Technology: Harness the power of technology tools and resources to streamline the narrative writing process. Digital platforms, reference management software, and writing assistance tools can enhance productivity, organization, and collaboration among team members.

Automation of Narratives

The automation of narrative writing offers promising opportunities to streamline and optimize the process. Natural language processing (NLP) algorithms, machine learning techniques, and artificial intelligence (AI) platforms can analyze data, generate insights, and draft narrative content with increasing accuracy and efficiency. While automation cannot replace human creativity and critical thinking, it can complement the work of medical writers by automating repetitive tasks and providing valuable support in data analysis and interpretation.

Tips for Narrative Writing

  • Know Your Audience: Tailor the narrative to the needs and preferences of the target audience, who could be healthcare professionals, researchers, policymakers, or patients.
  • Focus on Clarity and Simplicity: Use clear, concise language and avoid unnecessary jargon or technical terms. Ensure that the narrative is accessible and understandable to readers with varying levels of expertise.
  • Engage the Reader: Capture the reader’s attention from the outset with a compelling introduction and maintain engagement throughout the narrative with vivid storytelling and relevant examples.
  • Stay True to the Science: Uphold scientific integrity and accuracy in all aspects of the narrative, from data interpretation to citation of sources. Avoid sensationalism or exaggeration of findings.
  • Seek Feedback: Welcome constructive feedback from peers, mentors, or subject matter experts to improve the quality and effectiveness of the narrative.

Narrative writing in clinical research is a multifaceted endeavor that requires a combination of creativity, analytical rigor, and effective communication skills. By adhering to the guidelines outlined in this guide and embracing innovative approaches and technologies, medical writers can master the art of narrative writing and contribute to advancing scientific knowledge and improving patient care outcomes.

How to Avoid Procrastination in Scientific Writing & Publishing Process?

The complexity of research and the pressure to publish in prestigious journals can feel daunting, tedious, and frustratingly slow. This often leads to procrastinating and delaying working on manuscripts until the last minute. Procrastination is quite like a domino effect  leading to increased stress, lower quality work, and missed opportunities for publishing significant findings. Understanding the reasons for procrastination and implementing effective strategies is crucial for scientists to enhance their productivity and reduce the anxiety associated with the writing and publishing process. This blog explores practical tips to overcome procrastination in scientific writing and publishing.

Understand the root cause

Procrastination in scientific writing can be attributed to several factors:

Perfectionism: Many scientists feel their work is never quite ready, which leads to continuous revisions and delays.

Overwhelm: The sheer volume of data, literature reviews, and the complexity of thoughts that need to be organized can be daunting.

Fear of Failure: Concerns about rejection from journals or criticism from peers can hinder progress.

Lack of Clarity: Uncertainty about the paper’s structure or the research’s main message can cause delays.

Poor Time Management: Inadequate planning and prioritization can lead to last-minute writing under pressure.

Recognizing these triggers is the stepping stone toward addressing procrastination.

Strategies to Avoid

  1. Set Clear Goals and Deadlines

Writing a full scientific paper in one stretch can feel like an unsurmountable task. Unclear intention to “work on the paper” opens the door to endless procrastination. Instead, set specific goals like “complete the introduction by Thursday” or “have the first full draft done in two weeks.” Attach firm but reasonable deadlines to these goals and build accountability by sharing your timeline with colleagues or advisors. Clear objectives with target dates provide motivation and make procrastination more difficult. Additionally, break the mammoth task process down into a series of manageable steps:

  • Outline the paper and sections
  • Complete the Introduction section
  • Analyze data and create figures/tables
  • Write the Methods
  • Draft the Results carefully
  • Discuss the findings
  • Edit and refine

Focusing on one component at a time makes the workload less overwhelming. Do not forget to pat your back and celebrate small achievements along the way.

  1. Establish a Writing Routine

Consistency beats sporadic bursts of activity. Using the Pomodoro Technique often kicks in when facing long, unbroken stretches of work. The Pomodoro Technique helps counter this by splitting work into 25-minute focused sessions separated by 5-minute breaks. During each Pomodoro, commit to pure concentration on the writing task. When the timer goes off, take your break, reset, and go again. This system provides breaks to refresh while keeping procrastination at bay. While it may seem counterintuitive, building in true breaks completely separated from writing can renew focus and reduce the perceived need to procrastinate. Take a walk, exercise, read a book, or pursue a hobby — any activity offering a mental reset from the manuscript. Short periods of reprieve prevent burnout and frustrated procrastination.

Click Here:- The Evolving Role of Medical Writers: Adapting Content Management Systems

  1. Create a Supportive Environment

The environment in which you write can significantly impact your productivity. Choose a quiet, clutter-free space that encourages focus. Inform your colleagues or family about your writing schedule to minimize interruptions. Consider working at different times of the day when you feel most focused and energetic. An environment designed for concentration makes productive writing sessions much easier. The very reason famous authors like Rabindranath Tagore, Roal Dahl, and Richard Feynman had dedicated writing spaces or places where they felt motivated to write, successfully keeping procrastination at bay.

  1. Tackle the Hardest Tasks First

Begin with the sections of your manuscript that you find most challenging. This could be the results section where you need to interpret data or the discussion where you link your findings to existing literature. Completing the most difficult parts first can provide a significant motivational boost and make the remaining tasks feel more manageable.

  1. Use Writing as a Tool for Thinking

Don’t wait to start writing until you have all your thoughts perfectly aligned. Writing can be a formative process through which clarity and new ideas emerge. Start with rough drafts and don’t worry about perfection on the first go. This approach can help mitigate the paralysis often caused by perfectionism. Look for writing groups or clubs within your department or institution that meet regularly. These forums create external motivation and pressure to make progress. Groups also provide empathy, tips, and feedback from colleagues facing similar challenges.

  1. Limit Distractions

Identify what distracts you the most—emails, social media, or office noise—and take steps to mitigate these during your writing time. Tools like website blockers can help keep online distractions at bay while noise-cancelling headphones can be a boon in a noisy environment.

  1. Reward Yourself

Set up a system of rewards for meeting small milestones. For example, after finishing a draft of your methods section, treat yourself to a coffee break or a short walk. These little rewards can provide incentives and make the process more enjoyable.

  1. Seek Feedback Early

Don’t wait until your manuscript is fully written to seek feedback. Discussing your paper with colleagues or a mentor early in the writing process can provide new insights, catch potential errors, and significantly improve the quality of your work. This also helps keep the project moving forward and reduces the fear of criticism.

  1. Stay Physically and Mentally Healthy

Physical and mental well-being can significantly affect your ability to focus and write effectively. Ensure you are getting enough sleep, eating well, and engaging in regular physical activity. Mindfulness or meditation practices can also help manage stress and enhance concentration. This is a sure-shot way of fighting back the demon of procrastination.

  1. Learn from Rejections

View rejections not as failures but as opportunities to improve. Analyze reviewer comments carefully and use them to strengthen your manuscript before submitting it to another journal. Rejections are a great way to propel you to give your 100%, as they say, “Setback is by no means an excuse for procrastination, it is the platform for your best comeback”.

Procrastination is a challenge, but not an unsurmountable one. By understanding its causes and implementing structured strategies, scientists can overcome delays in their writing and publishing endeavors. Remember, the goal is progress, not perfection. Each small step forward is a victory against procrastination, bringing you closer to sharing your research with the world.

Turacoz Healthcare Solutions workshop

 

On 6th July 2018, Turacoz Healthcare Solutions organized an eventful and interactive workshop on “Best practices for Scientific Writing & Publications” in Canada. The workshop drew a gratifying response from diverse audiences and professionals.

The workshop was a synthesis of discussions, presentations and a one-on-one session on issues associated with creating an original research article, data sharing, publication writing, etc.

All sessions were highly interactive and informative. Dr. Namrata, Founder, Director & Trainer at Turacoz Healthcare Solutions went an extra mile to guide the participants on the technicalities of scientific & publication writing.

It is important for a research article to make the cut and at this workshop Dr. Namrata explained the ways one could accomplish this. The workshop also had career counselling sessions for aspiring medical writers along with the bilateral sessions, presentations & editing support for a drafted or rejected manuscript.

This workshop was a feat by Turacoz Healthcare Solutions to promote quality Medical/Scientific writing and Publication writing and to propel & steer endeavoring medical writers and researchers.

Chitkara University and Turacoz Healthcare Solutions Pvt. Ltd.: Memorandum of Understanding (MoU) and Centre of Excellence

On May 2018, Turacoz Skill Development Program (TSDP), a wing of Turacoz Healthcare Solutions signed a MoU with Chitkara University, Punjab, India for initiating training centers for pharma and life sciences freshers and train them as per the industry standards. The trainings would cover the requirements in different industries like medical communication companies, healthcare KPO/BPOs, journals, hospitals, pharma industry, healthcare event management companies, universities/colleges, etc. Turacoz Skill Development Program would run a Centre of Excellence within the University campus and provide paid internship to the students. It would also conduct faculty development programs and organize free seminars within the university premises

Turacoz Conducted a Workshop in 1mg, Gurugram (India)

Turacoz conducted a workshop on “Literature Search and Lifecycle of a Manuscript” in 1mg Technologies, Gurugram on 10th April 2018. The workshop was conducted by Dr Namrata Singh, Director and Vasudha, Lead Medical Writer of Turacoz. The sessions focused on types of publications, lifecycle of a manuscript, structure of a manuscript, and literature search. The participants really liked the workshop and had great interactions with the trainers.