Reliable writing partner through your drug success
Medical Writing Services
ADI Intellect provides a wide range of high-quality medical writing services for the Pharmaceutical, Biotech, and Medical devices companies across the Globe. Our team of qualified and experienced Medical Writers is experienced and equipped to write all range of Regulatory, Scientific, Clinical, and Marketing communication documents.
ADI Intellect Medical Writers can help you to prepare clear, concise, and high-quality documents and reports for Regulatory Submissions, publications in peer-reviewed medical journals and effective marketing communications. Our writers undergo continuous training with professional organizations. Not only do we meet your deadlines, but we provide high-quality deliverables in a cost-effective approach.
- 30+ years of experience in Regulatory Writing
- Experience across multiple therapeutic area
- SOPs across most documents and submission process
- Regulatory submission as per ICH E3 guidelines
- 100% Acceptance Rate
- Scalable business model
- 100+ successful regulatory/scientific writing projects
- Experience working on 100,000+ clinical trial analytics
Expert Medical Writing without Hassle
Clinical Study Report (CSR)
Maximize the effectiveness of your clinical study report and increase your chances of FDA approval. Your clinical trials report has to meet a complicated criterion and ascertain certain standards.
Protocol design development for your clinical trials is fundamental in the development of the project. Our services have been designed with this in mind and provide an accurate and bespoke designed protocol to ensure the progress into the clinical phase of drug development runs smoothly.
These offer a thorough analysis of pre and post-market clinical data in relevance to the intended use. The issues elicited as a patient narrative will be put across in a way so that you, as an existing or upcoming stakeholder in the concerned disease/medical condition, can draw considerable meaningful insight on the same.
Our dedicated team of bibliographical researchers gather relevant information from a multitude of subject areas, putting each individual search through an intensive data-filtration process. The researchers then condense expertly selected information into succinct, reviewer-friendly summaries.
Get it “write” the first time
Regulatory and Clinical Writing
- ICH GCP compliant Clinical Study Reports (CSRs); Phases I to IV, including CSR Synopses for public disclosure
- Study Protocols
- Clinical and non-clinical sections of the Common Technical Document (CTD) including summaries and overviews for EU and US Regulatory Authorities
- Investigator Brochures
- Patient Safety Narratives
- Patient information including Informed Consent and Patient Brochures
- Pharmacovigilance documents such as Periodic Safety Update Reports
- Standard Operating Procedures (SOPs) covering all aspects of drug development including the design, conduct, and reporting of clinical trials and the outsourcing of Sponsor responsibilities to a Clinical Research Organization (CRO)
- Conference materials (abstracts, poster presentations and slide sets)
- Editorial support
- Journal/conference submission
- Product website content (for both scientific and patient audiences)
- Educational material for patients, healthcare professionals and pharmaceutical industry personnel
- Medical marketing reviews and reports
- Literature reviews
- Publication planning
At ADI INTELLECT, we take pride in our process driven work culture. Following this practice for more than 15 years lends us an edge with niche expertise.
Trust & Accountability
With every service we seek to add value to your business undertaking. We have been delivering what we promised for the last fifteen years
We at ADI INTELLECT are focused simplistic! Our professionals work on the principal of precision, which is why we never lose focus in offering you custom services.
Driving Personal Growth
We not only place ethical practices on a pedestal, but also are thoroughly committed to offering career progression for those engaged with us.