RegGrow has the potential to assist you to begin and grow your career in the pharma, biopharma, Biotech, clinical, and medical devices industry. We offer post-graduation diplomas, certification, and education courses. RegGrow is envisioned for sustainable development of career paths for professionals and is the best professional academy in India and reaches a worldwide level creating the impetus for healthcare professionals.

RegGrow is a startup focused on the pharma and biopharma domain, providing education, training, and services to individuals and organizations in the industry. Its goal is to help people grow and develop their skills, knowledge, and expertise in various aspects of the pharmaceutical sector.

We deliver the perfect platform of content to students and professionals to help them achieve desired job opportunities and growth in the profession. One of the unique features of RegGrow is its focus on bridging the gap between academia and industry. The startup collaborates with universities and research institutions to offer training programs that provide practical skills and knowledge that are directly applicable to industry settings. We aim to develop regulatory professionals and expand their skills and knowledge in the Pharma, biopharma, Biotech, clinical, and medical devices industry throughout India and across the world. At RegGrow we ensure that you receive all the support, guidance, advice, and help as you navigate your professional journey.

The company offers a wide range of educational services, including online courses, workshops, seminars, and conferences, all designed to help individuals and organizations stay up-to-date with the latest trends and advancements in the field. RegGrow's team of experts ensures that its training programs are engaging, effective, and tailored to the specific needs of its clients.

RegGrow's services extend beyond education and training, providing consulting and advisory services to help individuals and organizations achieve their business goals. Its team of experienced consultants provides guidance and support in areas such as regulatory compliance, clinical trials, drug development, and market access.

RegGrow is committed to providing high-quality services that are grounded in scientific rigor and industry best practices. Its team is dedicated to helping individuals and organizations in the pharmaceutical sector achieve their goals by providing them with the knowledge, skills, and tools they need to succeed.

Overall, RegGrow is a dynamic and innovative startup that is poised to make a significant impact in the pharmaceutical industry. Its focus on education, training, and services reflects its commitment to driving growth and development in the field while ensuring that its clients are equipped with the expertise needed to excel in their careers.

Who can register:

• BSC/MSc (micro, chem, bio, biotech, medical devices, clinical, bioanalytical, etc.)

• BHMS/BAMS

• B. tech/ M. tech

• B. Pharma/M. Pharma

• PhD

• Professors

• Experience professional

Academics:

• Providing certification courses to pharmacy and life science colleges like Regulatory Affairs, clinical research, pharmacovigilance, etc.

• We are ready to do MoU with colleges for audit purposes.

• Offering PG diplomas for life science, paramedical and pharmacy students for a different segment on current need.

• Arranging one-day or two-day seminars or workshops for the colleges on any topic suggested by the colleges.

• Providing consultancy services for the pharma and life science industry and academics.

• Providing experts from different domains as Guest lectures to the colleges to build the skills of students and teachers.

Industry :

• Preparation and compilation of all modules (1 to 5 ) in eCTD, Nees, and ACTD format.

• Writing the summaries for Drug product and Drug substance

• Writing of clinical summaries (2.7.1 US/EU, BTIF, customer requests, etc.)

• US labeling section preparedness

• Presubmission support for controlled correspondence, pre-ANDA meetings, post-CRL meeting requests, etc.

• Post approval support for CB-0, CBE-30 and PAS submission.

• Preparation & writing of clinical study protocol, clinical study report, and bioanalytical report and its appendices