Our regulatory affairs consultants can help you in all areas of international regulatory affairs relating to medicines, medical devices and other healthcare products in all the major territories of the world.
Our team of highly experienced regulatory affairs consultants can help you, whether it involves:
- Regulatory planning for a future submission;
- Advice on international regulatory requirements;
- Writing or reviewing a dossier;
- Troubleshooting an unsuccessful submission or conducting an appeal;
- Liaison with the regulatory authorities;
- Maintenance of regulatory approvals throughout their life cycle.