Achieva Global Meetings has an extensive background in clinical meeting planning. Our clients include pharmaceutical companies, clinical research organizations, biomedical technology companies and medical device and equipment corporations.
We are experts in every component of the clinical trial process, from conception to completion of multi-year studies. We consistently research changing health industry policies and regulations so we remain compliant with current industry standards. We work closely with you to implement your company’s regulatory procedures and guidelines.
We can put together successful programs whether in the United States or countries beyond our borders; we have played a critical role in producing global studies for our clients.
Our highly experienced and well trained staff provides the ultimate in confidentiality and knowledge of the client code of ethics. Our on-site teams are trained on PhRMA guidelines, FDA regulations and Sunshine Act Reporting.
- Product Launches
- Investigator Meetings
- Advisory Boards
- CRA Training
- Speaker Rehearsal
- EDC Training
- Protocol Review Meetings
- Investigator Dinners