The high cost of compromise: Why patient safety must come first
Dr Ranjit Barshikar, CEO – QbD International, United Nations Advisor cautions that India’s reputation as the ‘Pharmacy of the…
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Revised Schedule-M
FOPE & PharmaState Academy advance MSME excellence with PULSE session 24 on contract management
Industry leaders underscore the vital role of contract management in ensuring compliance, sustainability, and global…
Session 21 of FOPE, PharmaState Academy’s PULSE Program, advances excellence in manufacture of APIs…
The keynote address was given by Namit Joshi, Chairman, Pharmexcil, followed by the expert educator session by Dr Jitender…
FOPE, PharmaState Academy’s 16th PULSE Session held on Oral Liquids manufacturing under Revised…
The session opened with a keynote address by Dr Viranchi Shah, followed by an education segment led by Abhijit S. Kulkarni, VP CQA…
What the new drug rules mean for quality control in Pharma: From lab to license
Dr Saurabh Arora, Managing Director, Auriga Research, explains how prioritising integrity, infrastructure, digital systems, and…
FOPE and PharmaState Academy conduct session on sterile drug manufacturing under Revised Schedule M
Session 18 of the PULSE initiative focuses on regulatory compliance, operational standards, and technical readiness in sterile…
FOPE & PharmaState Academy conducts session 17 on gap analysis and implementation plan for…
A structured and well-documented Gap Analysis is essential for identifying deficiencies, strengthening compliance, and ensuring…
Understanding opportunities and challenges for SMEs after breather on Schedule M deadline
Akshansh Chaudhary, Executive Director & Chief Technical Officer, Venus Remedies highlights the challenges SMEs face and how…
Pharma MSMEs ask for condition-free time frame of 2-3 years to implement revised Schedule M
In a letter to the Union Health Ministry, Small & Medium Pharma Manufacturers Association stated that pharma MSMEs are not…
Revised Schedule M implementation for MSMEs extended, industry welcomes move
The timeline of implementation is extended till December 31, 2025 but pharma MSMEs must file an application with the Central…