maximize your Submission success rate with our medical writing expertise!

With our track record of success in medical writing,   MARS - Global are convinced that we can help you reach your objectives and increase your submission success rate by offering top-notch material that satisfies the highest quality and excellence requirements.

Why work with mARS- Global medical writing team?


We realize the necessity of providing high-quality material that fulfils healthcare industry strict standards on our medical and regulatory writing team. Our professional and highly skilled writers, editors, and regulatory specialists work together to deliver complete services that meet your demands.

Confidentiality

MARS-Global respect the sensitive nature of medical and regulatory writing projects and ensure complete privacy throughout the process.

Timely Delivery

MARS-Global has a history of never missing a deadline. Indeed, we are known to pre-enroll with the highest quality.

Competitive Pricing

MARS-Global provides competitive pricing without compromising the quality of the services, so you can be certain that you will get the most potential return on your investment.

MARS-Global Medical Writing Services

"Optimizing Clinical Trials for success: from protocol Development to quality control and regulatory compliance"

 

  • Protocol development tailored to specific needs, ensuring study design, endpoints, and statistical analysis plans are optimized for success.
  • Creation of comprehensive clinical study reports (CSRs) that meet regulatory requirements and accurately document the results of clinical trials.
  • Development of investigator brochures that provide detailed information on the drug or medical device being tested, including safety, pharmacology, and clinical trial results.
  • Assistance with the development of regulatory documents required for clinical trial applications, such as Investigational New Drug (IND) applications, New Drug Applications (NDAs), and Marketing Authorization Applications (MAAs).
  • Expert guidance and advice on medical writing projects, including study design, data interpretation, and regulatory compliance.
  • Assistance in writing grant proposals for funding of clinical research studies, including preparing budgets and timelines.
  • Quality control services, including editing and proofreading to ensure documents meet high standards for accuracy, clarity, and compliance with regulatory requirements.
  • Facilitation of the development of consensus statements by summarizing the findings of expert panels and facilitating discussions to reach a consensus on key issues.
  • Creation of key intelligence toolkits that summarize relevant literature, competitive landscape, and regulatory requirements to inform product development strategy.
  • Preparation of comprehensive meeting minutes for advisory board meetings, ensuring accurate and complete documentation of discussions, decisions, and action items.
  • Manuscript preparation services, including preparation of clinical trial reports, review articles, and case reports for publication in peer-reviewed medical journals.
  • Creation of compelling slide decks and other materials for scientific presentations at conferences, symposia, and other events
  • Development of educational materials for healthcare professionals, including patient education materials, and training manuals.

stay ahead of the curve !

with our cutting-edge medical writing services 

"Examples of MARS-GLOBAL's prior work"

Customers served! 100 MEDICAL WRITING CONSULTATION

What Our Clients Say

Highly recommend. Fast turn-around, great prices and quality writing. As a medical services company, it was great to be able to outsource some writing projects to a company that could “speak the language”.

Dr. Mohsen Fathallah, M.D., Ph.D.
CEO & Managing Director, Genuine Research Center GRC. 

It’s indeed pleasure to work with MARS team, and I hope there’s future opportunity for collaboration.

I highly recommend all to approach MARS for any work without second thoughts.

Prof. Dr. Muhammad Yazid Jalaludin.
Deputy Dean (undergraduate studies), Faculty of Medicine, University of Malaya

experience the power of professional academic and regulatory medical writing!

Join more than 2,000 clinical researchers.

>