Ensuring Drug Safety and Efficacy
Develop and manufacture medicines that are safe, effective, and high quality. Rigorously test all products through preclinical and clinical trials following CDSCO (Central Drugs Standard Control Organization) guidelines. Continuously monitor and report any adverse effects (pharmacovigilance).
Regulatory Compliance
Adhere to national regulations like the Drugs and Cosmetics Act, 1940 and rules made thereunder. Ensure timely approvals from agencies like CDSCO, DCGI (Drugs Controller General of India). Maintain compliance with GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices).
Ethical Business Practices
Promote medicines ethically without making false claims. Follow strict codes of conduct for marketing and interactions with healthcare professionals (as per the Uniform Code of Pharmaceutical Marketing Practices - UCPMP). Avoid conflicts of interest and prioritize patient welfare over profits.
Affordable and Accessible Healthcare
Work towards making medicines affordable for all sections of society. Partner with government and NGOs for public health initiatives. Support the development and distribution of generic medicines to improve access.
Transparency and Accountability
Provide clear and complete information about drugs, including side effects, dosage, and risks. Disclose clinical trial data as required by Indian and international standards. Be open with stakeholders — regulators, healthcare providers, patients, and the public.
Environmental Responsibility
Ensure environmentally sustainable manufacturing processes. Properly treat pharmaceutical waste to prevent environmental contamination. Minimize carbon footprint and resource wastage in production and packaging.
How it works
Three Easy Steps
1
Research and Development (R&D)
Scientists research diseases and create new medicines or improve existing ones.
New drugs go through strict laboratory tests and clinical trials to check safety and effectiveness.
2
Manufacturing
Approved medicines are manufactured in factories that follow strict quality and safety rules (GMP).
Every batch is tested to maintain high standards before reaching the market.
3
Post-Market Surveillance
Even after a drug is available, companies monitor it for any side effects.
Any issues are reported to the authorities, and corrective actions are taken if needed (pharmacovigilance).
Affordable and Accessible Healthcare
- Affordable and widely available medicines help improve the overall health of the country, increase trust in the company, and fulfill an important social responsibility.
Research and Innovation
- Research and innovation help the company stay competitive, meet urgent healthcare needs, and bring better health solutions to society.
