We offer a full spectrum of services

Our years of experience include writing, rewriting, ghostwriting, researching, fact-checking, editing, proofreading, wordsmithing, reviewing, and referencing:

• Regulatory documents (all-phase clinical trial protocols and reports, patient narratives, clinical development plans, IND and NDA annual reports and submission components)
• Integrated summaries of safety and efficacy (ISS and ISE)
• Investigator brochures and annual updates
• Manuscripts and abstracts for publication in scientific/medical journals
• Phase IV and post-marketing materials
• Patient and physician education materials
• Literature searches and reviews
• On-site medical meeting/advisory board coverage
• Executive summaries
• Competitive information monitoring and analysis
• CME materials

 

Areas of Expertise

Analgesics

Antibiotic Resistance

Antifungals

Antivirals

Cardiovascular Disease

Cold Products

Endocrine Disorders

Erectile Dysfunction

Infectious Disease

Infertility

Medical Devices

Movement Disorders

Neurology

Oncology

Oral Hygiene Products

Urology