Convex CRO has extensive experience with regulatory submission of documents for clinical trials authorization by the Bulgarian Drug Agency (BDA), Ethics Committee for Multicenter Trials (CEC) and/or Local Ethics Committees (LECs). Our regulatory services include:
- Regulatory consulting
- Creation, compilation, review and adaptation of regulatory documentation
- Communication with RA and EC
- Submission of regulatory files
- Maintenance of regulatory files post-approval
Whether we are providing expert advice, planning meetings or facilitating communication between the sponsor and the BDA/CEC/LEC, we guide our clients through each step of the approval process by providing unsurpassed regulatory services. All this leads to smooth and faster startup of any trial.