Medical Device Company
AML Christensen will work closely with you and deliver accurate, timely and cost effective documents of a high ethical and scientific standard.
AML Christensen will be the extension of your team by being flexible to your scope, demonstrate the efficacy of your medical device and improve patient safety. All documents produced by AML Christensen can undergo quality control review.
We can assist you with:
Clinical and Regulatory writing
- Brochures for investigators
- Study protocols
- Patient information including full informed consent and brochure
- Consentand Patient Brochures
- Clinical summaries of safety and efficacy
- Clinical evaluation report (CER)
- Conference materials (abstracts, posters and PowerPoint slide sets)
- Education material for patients, healthcare professionals and medical device industry personnel
- Medical marketing review and reports