Services offered by Peter Meade Scientific Writing Ltd include:
Authoring of regulatory and non regulatory documents in in-house or submission standards.
Medical writing editorial review and QC of regulatory documents.
Clinical Study Protocols and Amendments

Clinical Study Reports (CSRs)

Lay Person Reports

Investigator Brochures, updates and addenda (IBs)

Patient Safety Narratives

Regulatory Submission Documents (eCTD modules - both clinical and nonclinical phases)

Periodic Safety Reports and drug Safety Update Reports (PSUR/DSURs)

Summary Bridge Reports

Nonclinical reports

Paediatric investigation plan (PIP)


Nonclinical reports

Journal articles

Review articles for scientific web sites.