Regulatory, Compliance, and More.GAP extends its expertise from operation to management of clinical study/trial with early cost effective and product delivery basis. GAP has a panel of experts to deal from regulatory approval to submission of results for market authorization. Our experienced and knowledgeable staff will assist you in following areas:
- Clinical trial- Participant Rights and Notifications
- Clinical trial- Study Conduct
- Clinical trial- Start Up Activities
- Ongoing Clinical Trial Activities
- Clinical trial- Close out
- Clinical trial – Study Files
- Clinical trial – Supplies
- Laboratory Records and Specimen Retention
- Contact us for more information.