Medical Writing

Regulatory Consulting (human drug studies)

Regulatory Consulting (medical devices)

Study Start-up

Monitoring

Project Management

Medical Writing

Project Rescue

Medical Writing

For any kind of documents required in a study, you have to be aware of local and international regulations. Our medical writers have experience in drafting documents required in both human drug and medical device studies:

• Clinical study protocols / clinical investigation plans
• Informed consent forms
• Information material for patients, investigational sites or for promotional purposes
• Investigator’s brochures
• Manuals, instructions for use, SmPCs
• IMPDs
• DSURs/PSURs
• Clinical study reports, publications, posters

All documents can be translated into local languages by our translation service.

• Address:
  MEDICRO GmbH
  Klostersteig 19
  D-91580 Petersaurach
• Telephone:
  +49 9872 9699027
• Fax:
  +49 9872 9699029