Are You Looking For Expert Medical Writing?
We are a team of experts having 20 years of Industrial experience in regulatory affairs. We have written scientific content for website, blogs, clinical reports, and observation studies. Connect with us to know more.
- Scientific Content Writer
- Excellent Medical Writing
- Completed 50 Plus Medical Writing Projects
Medical Writing Services
Our Medical Writing Services:
Regulatory Medical Writing Services
We specialized in high quality structured and accurate regulatory documents including Investigational New Drug (IND), New Drug Application (NDA), Common Technical Document (CTD), Electronic Common Technical Document (eCTD, Risk Management Plan (RMP), Pharmacovigilance Safety Update Report (PSUR) and many more. From pre-clinical studies to post marketing surveillance, we prepare detailed submission ready documents.
Medical Writing For Clinical Trials
We support clinical research activities with impactful clinical documents at every stage/phase of clinical trials. Our experts assist you with preparation of Clinical Trial Protocol, Investigational Brochure, Clinical Study Reports, and Informed Consent Form. We combine scientific and technical knowledge for preparation and compilation of clinical medical writing.
Medical Writing Consultancy Services
Our medical writing consultancy services includes online consultation about clinical documentation and submission of clinical documents. With our expertise in medical writing, you can avoid unwanted errors and mistakes in your clinical and regulatory documents. Minimum errors and compliance documentation results in timely approvals.
Training and Medical Writing Support
Our medical writing support extends from self scientific and technical documents preparation to providing training to your team in regulatory and clinical documentation best practice, ensuring compliance with regulatory standards.
Why Choose Medwisdom Lifescience For Medical Writing Services?
Unmatched Expertise
Our team has experienced medical writers, regulatory specialist, and clinical researchers who understand the global regulatory requirements and framework, that helps to avoid non-compliance.
Extensive Service
We provide broad range of medical writing services from drug development to post marketing surveillance, we offers end to end documentation solution for pharmaceuticals, medical device, and cosmetics.
Global Regulatory Compliance
All documents are aligned with the regulatory authority requirements like USFDA, EMA, CDSCO, ICH, and country specific guidelines.
On Time Delivery
We ensure timely medical writing services for pharmaceutical, medical device service for clinical trials, and regulatory medical writing without compromising the quality.
Industries We Serve
Pharmaceutical Companies
We provide support in drug development, scientific writing for clinical studies, and regulatory submission.
Biotechnology
We help you prepare scientific content for groundbreaking innovative research.
Medical Device
Creating technical and compliance documents for medical device.
Healthcare Organizations
Provide support for clinical research and publication for healthcare organizations.
Let’s Work Together
At Medwisdom Lifescience, we are dedicated to deliver high quality, research driven medical writing services that could exceed your expectations. By choosing us, you are not choosing only medical writer, you are gaining a partner committed to helping your product enters market faster, with unmatched quality.
Reach out to us today, to know how our clinical medical writing services and regulatory medical writing expertise can help you to transition your challenges into success stories.
What Our Clients Think About Us
Frequently Asked Questions
What Is Regulatory Medical Writing?
Regulatory medical writing involves creating scientific and technical documents such as clinical trial protocol, clinical study report, and risk management plan required by the regulatory authorities for submission in order to acquire product registration.
How Does Medical Writing Support Clinical Trials?
Medical writing supports clinical trials by documentation of clinical study design, progress report, and results analysis. It ensures the clinical data is accurately presented with regulatory compliance.
What Are Medical Writer Consultancy Services?
Medical writer consultancy services includes guidance and support to individual or organization that needs help with scientific and technical documents with regulatory compliance of specific countries. It also includes content creation for clinical trials and regulatory submissions.
How Medical Writing Can Improve Regulatory Affairs Submissions?
Professional medical writers ensures scientific and technical documents they have created are accurate and precise meeting compliance of regulatory authorities. All the documents format are well structured and high quality standard, ensuring fast and effective regulatory submissions.