Services

We provide end-to-end regulatory support for Bioavailability & Bioequivalence (BA/BE) studies and clinical trials, ensuring compliance with national and international guidelines. Our services include regulatory submissions, dossier preparation, and liaison with drug regulatory authorities.

 GIEC offers specialized research services for academic research papers and other scientific publications, assisting researchers in study design, data analysis, and manuscript preparation.

We support researchers in journal paper submission, editing, and publication across reputable scientific journals, ensuring high-quality content that meets international publishing standards.

GIEC has established strategic partnerships with hospitals where clinical trials are conducted, facilitating ethical approvals, compliance monitoring, and seamless research execution.

With a strong commitment to ethical integrity and research excellence, GIEC continues to be a trusted partner in advancing clinical and pharmaceutical research.

  For BA/BE and clinical trial sites that do not have an in-house Ethics Committee, GIEC provides independent ethics review and approval services, ensuring compliance with ethical and regulatory guidelines.