by admin

Clear, concise, and professional presentation of study findings is an important factor in any development program. With a full complement of medical and scientific writing services, Wizard Clinical professionals can provide all your documentation and writing needs. Comprised of scientists, many with advanced degrees, Wizard scientific and medical writing team has significant expertise in key therapeutic areas of pharmaceutical and biotechnology clinical development. They work directly with you to ensure consistency with your format and style while maintaining full compliance with regulatory requirements and International Conference on Harmonisation (ICH) guidelines. Wizard has a proven track record of timely delivery of quality medical writing deliverables coupled with outstanding customer service.

Wizard scientific and medical writing team consists of writers, editors, and writing management staff. Most of the writers are regulatory focused by training and prepare documents related to clinical trial conduct, reporting, and regulatory submissions. Most of our medical writing staff have therapeutic experience in neuroscience, oncology, cardiovascular, critical care, autoimmune, diabetes/endocrine, infectious disease, men’s health, women’s health, and osteoporosis/bone metabolism areas and are located in North America and we also have resources in India.

  1. Protocols and protocol amendments
  2. Informed Consent Forms/Patient Information LeafletsT
  3. Clinical study reports
  4. Subject narratives
  5. Investigator Brochures
  6. Integrated summaries of safety/efficacy
  7. Literature summaries
  8. Clinical expert reports
  9. INDs, NDAs, BLAs, CTAs (Module 2) summary documents
  10. IND and NDA Annual reports
  11. Safety Aggregate Reports (PSURs, PADERS, Line Listings, DSURs)
  12. Clinical trial registry synopses
  1. Manuscripts
  2. Abstracts
  3. Posters
  4. Symposia publications
  5. Slide presentations
  6. Publication plans