BNPedge




The Medical Writing Services group at BNPEDGE is well versed to write, edit, organize, and deliver a wide range of medical and scientific documentation.

Our core portfolio includes Study Protocols, ICH GCP compliant clinical study reports (CSRs); Phases I to IV, Clinical trial.gov updates for public disclosure, Clinical sections of the Common Technical Document (CTD) including summaries and overviews, Investigator Brochures, Patient safety narratives, Pharmacovigilance documents such as Periodic Safety Update Reports (PSURs) and Development Safety Update Reports (DSURs), Standard Operating Procedures (SOPs) covering all aspects of drug development including the design, conduct and reporting of clinical trials, Initial Pediatric Study Plan (iPSP), Failure Mode Effects and Criticality Analysis (FMECA) and FMEA.


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BNPEdge provides Regulatory guidance covering:

FDA Meeting Guidance(EOPI/II, Pre-NDA)
505(b)(2) submissions
Orphan Drug Designation Requests
Fast Track Requests
Regulatory Due Diligence
Regulatory Strategy in CNS, Dermatology, Respiratory, and Cardio-Renal therapeutic arenas

What We Offer

Services

What We Offer

Process Identification

one liner definition!

Legacy Application Integration

one liner definition

Regulatory and Clinical Writing Services

one liner definition

Onsite/Offsite Training

one liner definition

What problem are we solving?

Operational Costs
Productivity
Compliance
Risk
Customer Experience

Portfolio

Case Studies

Contact Us

Phone

1-732-476-6338

Email

info@bnpedge.com