Name of Department:  Faculty of Pharmacy in collaboration with IIC and IQAC

Organizer: Faculty of Pharmacy in collaboration with IIC and IQAC

Activity Incharge: Navdeep Singh

Date of Activity: 12.11.2025

Time: 11:00 am onwards

Aim or Objective:

• To gain knowledge about the concept, scope, and importance of cGMP in the pharmaceutical industry.
• To understand the regulatory guidelines provided by agencies such as USFDA, WHO, and EMA for CGMP compliance.
• To study the key components of cGMP including personnel, premises, equipment, documentation, and quality control.

Report:

One Day Workshop in Pharmaceutical Industry is held on the theme current Good Manufacturing Practice Day Placebo Club, School of Pharmacy, S. Lal Singh Memorial College of Pharmacy and Mata Jarnail K College of Pharmacy in collaboration with IIC and IQAC, Desh Bhagat University, Mandi Gobindgarh organized an  lecture on 12th October 2025. Mr. Som Gupta, General Manager in HNE healthcare Pvt. Ltd. In Panchkula is the speaker.

The speaker focused the importance of current Good Manufacturing Practice. Quality by design, risk management and assessment, critical process parameters, critical quality attributes, critical quality management, Role of Quality Assurance, Quality Control were well explained by the speaker.

There was an interactive question-answers session between the speaker and students at the end of the talk.

All the faculty members and students of Faculty of Pharmacy learnt a lot from this excellent lecture.  It was such a wonderful and knowledgeable lecture. Moreover students were made aware about current Good Manufacturing Practice and its importance in Pharmaceutical Industry.

Dr. Puja Gulati ended the session with a vote of thanks to the eminent speaker.

Outcomes:

1. Participants gained a comprehensive understanding of the importance and implementation of Current Good Manufacturing Practices in the pharmaceutical industry.
2. Students became familiar with global regulatory standards such as WHO, USFDA, and EMA guidelines.
3. The session enhanced awareness about quality assurance, documentation, and process validation in drug manufacturing.
4. Learners developed insight into practical challenges and solutions in maintaining product quality and safety.
5. The expert talk motivated participants to incorporate cGMP principles in their academic projects and future professional practices.