Brief overview>

Our Regulatory writing professionals comprises of Pharm.D., M.D., Ph.D. and master’s with good technical knowledge and diverse subject expertise ensuring preparation of a wide range of dossiers and reports.

Professional efficiency

The professional team of medical/ regulatory writers are experienced in producing high quality medical and related documents.. All write-ups are reviewed with regular consultation with the experts to produce scientifically sound documents as per client needs and technical legalities. Timeline is largely respected to ensure quick processing through various regulatory bodies.

Quality

All documents are reviewed through a strenuous process to ensure high quality document production. The accuracy, scientific logics and grammatical/typographical errors are thoroughly reviewed to preclude any possible errors. The appropriate style of writing such as such as the AMA Manual of Style and the Oxford Style Manual in accordance with the standard rules or company’s requirements are followed. Editorial reviewers have certification from the Board of Editors in the Life Sciences.

Support and assistance

Professional support, Subject expertise, efficient review team, and national and international collaboration ensuring high throughput data generation and support throughout the entire product life cycle.

Regulatory Submissions	Regulatory Writing/Medical Writing	Miscellaneous
Regulatory Submissions	Medical Writing	Regulatory Support Service
Drug	Clinical Writing	Project Management
Medical Divices/IVD	Dossier Writing	Career/Job Portal
Food	PSUR	Regulatory Auditing
Cosmetics	Academic Writing	Pre Approval Services
Vaccines/Biologicals