Corona Remedies secures ANVISA GMP certification for Brazilian exports
- Corona Remedies received ANVISA GMP certification for OSD and hormone facilities
- Certified units are located at Bhayla, Ahmedabad
- Approval enables exports to Brazil, a key Latin American healthcare market
- Disclosure made to BSE and NSE on October 22, 2026

*this image is generated using AI for illustrative purposes only.
Corona Remedies has received Good Manufacturing Practice (GMP) compliance certification from the Brazilian Health Regulatory Agency, ANVISA. This approval covers the company's oral solid dosage (OSD) and hormone manufacturing facilities located at Bhayla, Ahmedabad.
The certification marks a significant regulatory milestone for the pharmaceutical manufacturer. By securing compliance from ANVISA, the company strengthens its position for exporting medical products to the Brazilian market, one of the largest healthcare markets in Latin America.
Regulatory Details
The disclosure was made to the BSE Limited and National Stock Exchange of India Limited on October 22, 2026. The company cited Regulation 30 of the Securities and Exchange Board of India (Listing Obligations and Disclosure Requirements) Regulations, 2015, as the basis for this intimation.
Facilities Certified
The GMP certification applies specifically to two distinct manufacturing units within the Ahmedabad complex:
- Oral Solid Dosage (OSD) facility
- Hormone manufacturing facility
Both facilities are situated at Bhayla, Ahmedabad. The certification ensures that these units meet the stringent quality standards required by Brazilian health authorities for drug importation and sale.
Historical Stock Returns for Corona Remedies
| 1 Day | 5 Days | 1 Month | 6 Months | 1 Year | 5 Years |
|---|---|---|---|---|---|
| +0.45% | -1.44% | -8.27% | +25.88% | +41.13% | +41.13% |
How will the ANVISA certification specifically impact Corona Remedies' revenue mix from Latin American exports in the next fiscal year?
What specific hormone-based products is Corona Remedies planning to launch in Brazil following this regulatory approval?
Does this certification pave the way for similar GMP approvals from other major regulatory bodies like the US FDA or EMA?


































