Learn Revised Schedule M
– A Series of 26 Online Live Learning Sessions
Organizers:
Session -17 Sponsor:
- One of the leading names in the packaging industry
Knowledge Partner
Media Partner
Supporting Associations
- IPPMA – Indian Pharma Machinery Manufacturers Association
- CiPi – Confederation of Indian Pharmaceutical Industry
- Laghu Udyog Bharati -लघु उद्योग भारती
- KDPMA – Karnataka Drugs & Pharmaceuticals Manufacturer’s Association
- FMPCCI – Federation of Madhya Pradesh Chamber of Commerce & Industry
- HDMA – Himachal Drugs Manufactures Association
- RPMA – Rajasthan Pharmaceutical Manufacturers Association
- The Pharmaceutical Manufacturers Association Of Tamilnadu
- dma – Drug Manufacturers Association
- DMMA – Drug Marketing & Manufacturing Association
BOOK YOUR PACKAGE with Gap Analysis Session
Get access to "Gap Analysis session" as per Revised Schedule M + All upcoming sessions @Rs. 5000 + 18% GST per participant.
Individuals can book seat at link mentioned below.
For Group Bookings/Queries Contact or WhatsApp at +91-7011796683 on this number or by Clicking here>>>
Seat Booking Open For Session 24
Have you booked your seat?
Session 24: Management of Essential Contracts in Pharmaceutical Manufacturing
Date: 24th August (Sunday), 10:30 am - 12:30 pm
- The booking is now open for all session registration as one-time payment.
- You can make a one-time payment to book all sessions & their certification.
- In case you want to attend a particular session, you can make payment of that session in “Single Session” option.
Get 10% Exclusive discount for booking 5 or more seats, if you are a Member Company of any of the supporting associations mentioned below:
- Confederation of Indian Pharmaceutical Industry (CiPi), Laghu Udyog Bharati (LUB), Indian Pharma Machinery Manufacturers’ Association (IPMMA), Karnataka Drugs & Pharmaceuticals Manufacturer’s Association (KDPMA), Himachal Drug Manufacturers Association (HDMA), Federation of Madhya Pradesh Chamber of Commerce & Industry (FMPCCI), Drug Marketing & Manufacturing Association (DMMA), Rajasthan Pharmaceutical Manufacturers Association (RPMA), The Pharmaceutical Manufacturers’ Association of Tamilnadu, Drug Manufacturers Association (DMA), Federation of Pharma Entrepreneurs (FOPE).
- Click here to Connect on WhatsApp> for the association member company discount.
Note: Discount only for association member companies and on more than 5 seats booking.
Book Seat for Upcoming Session 24
- Attend: Live Session at ZOOM Platform.
- Included: Certificate & Session Recording.
Book Full Package
- Attend: All Upcoming Sessions.
- Included: Access to all Earlier & Upcoming Session Certificates & Recordings.
- Attend: Live Session at ZOOM Platform.
- Not Included: Certificate & Session Recording.
In case you want to Book Seat for any particular session, then make the payment for that particular session.
In case you want to Book Seat for any particular session, then make the payment for that particular session.
- Single Session Fee/Participant: Rs. 500 + 18% GST = Rs. 590/-
Includes:
- Exclusive WhatsApp Group.
- In-depth Q&A Sessions.
- Gap Assessments.
- Quiz Competitions (with Prizes), Case-Studies.
- Attend the live session for which the payment is made.
- Certificates of session.
- Get access to live session recording as the course for 2 months.
1 to 4 Seats (Fee/Participant)
-
Exclusive WhatsApp Group
-
Indepth Q&A Sessions
-
Gap Assessments
-
Quiz Competitions (with Prize), Case-Studies
-
Attend all upcoming sessions
-
Certificates of Earlier & All Upcoming Sessions
-
Recordings of Earlier & All Upcoming Sessions as Courses (access as soon as it is uploaded at website)
-
Get the Package access of all recordings as courses for 14 months
-
Exclusive References on Topics which will act as Ready Reckoner for Participants
5 to 10 Seats (Fee/Participant)
-
Exclusive WhatsApp Group
-
Indepth Q&A Sessions
-
Gap Assessments
-
Quiz Competitions (with Prize), Case-Studies
-
Attend all upcoming sessions
-
Certificates of Earlier & All Upcoming Sessions
-
Recordings of Earlier & All Upcoming Sessions as Courses (access as soon as it is uploaded at website)
-
Get the Package access of all recordings as courses for 14 months
-
Exclusive References on Topics which will act as Ready Reckoner for Participants
>10 Seats (Fee/Participant)
-
Exclusive WhatsApp Group
-
Indepth Q&A Sessions
-
Gap Assessments
-
Quiz Competitions (with Prize), Case-Studies
-
Attend all upcoming sessions
-
Certificates of Earlier & All Upcoming Sessions
-
Recordings of Earlier & All Upcoming Sessions as Courses (access as soon as it is uploaded at website)
-
Get the Package access of all recordings as courses for 14 months
-
Exclusive References on Topics which will act as Ready Reckoner for Participants
1 to 4 Seats
-
Private WhatsApp Group
-
Attend all upcoming sessions
-
Certificates for all upcoming sessions
-
Get access to live session recording as course for 1 month
Register without Certification
-
Certificate Not Included.
-
Attend live session.
Why should you attend?
Stay Ahead of Regulatory Changes: With the revised Schedule M, India’s pharmaceutical industry is embracing stringent GMP standards that align with global best practices. Attending this session ensures you understand these critical updates and can implement them effectively, maintaining compliance and avoiding costly regulatory setbacks.
25 In-Depth Online Sessions Covering Revised Schedule M:
Note:
- The sessions are planned on Sundays & the dates mentioned below are tentative. If there are any changes in dates the same will be communicated to you before the session.
- A special certificate will be awarded to professionals who attend all the sessions.
Date: 24th August | Sunday 10:30 AM IST
Educator
Dr. Sanjit Singh Lamba
Managing Partner, Trillyum Consulting
Chief Guest
Mr. Sunil Attavar
Chairman – Group Pharmaceuticals Ltd.
Q & A + Panel Discussion
Panelist
Mr. Subbarao Chinni
Managing Director, Crius Group of Companies
Panelist
Dr. Sanjit Singh Lamba
Managing Partner, Trillyum Consulting
Panelist
Mr. Akhlas Ahmed
Head – Supply Chain and New Developments, Mankind Pharma Ltd.
Date: 13th July | Sunday 10:30 AM IST
Chief Guest: Mr. Sunil Attavar, Chairman – Group Pharmaceuticals Ltd.
Session Educator: Dr. Sanjit Singh Lamba, Managing Partner, Trillyum Consulting.
Panel Discussion:
Dr. Deepak Haldankar, Pharma manufacturing leader,
40+ years of proven success in Quality (Formulation/API).Mr. Akhlas Ahmed,Head – Supply Chain and New Developments, Mankind Pharma Ltd.
- Dr. Sanjit Singh Lamba, Managing Partner, Trillyum Consulting.
Date: 25th May | Sunday 10:30 AM IST
Chief Guest: Mr. Milan Patel, Joint Managing Director, Troikaa Pharmaceuticals Ltd.
Session Educator: Mr. Abhay Kumar Srivastava, Senior President – Operations, Mankind Pharma Limited.
Panel Discussion:
Mr. Rajesh Kapoor, 25+ Yrs in cGMP & Compliance, Pharma Compliance Expert, Regulatory Trainer.
Mr. Digambar Nigade,Vice President – Quality Injectable, Amneal Pharmaceuticals.
- Mr. Abhay Kumar Srivastava, Senior President – Operations, Mankind Pharma Limited.
Date: 11th May | Sunday 10:30 AM IST
Chief Guest: Mr. Namit Joshi, Commercial Director, Centrient Pharmaceuticals & Chairman, Pharmexcil.
Session Educator: Dr. Jitender Khurana, International GMP Consultant: Quality System, Auditing, FDA Remediation and Training.
Panel Discussion:
Dr. Ajay Shrivastava, Site Head – Global API Business
SUN Pharma, Panoli.Dr. Sanjit Singh Lamba,Managing Partner, Trillyum Consulting.
- Dr. Jitender Khurana, International GMP Consultant: Quality System, Auditing, FDA Remediation and Training.
Date: 27th April | Sunday 10:30 AM IST
Chief Guest: Shri Kamal Chawla,Head of the Office, Controlling Authority/Deputy drugs controller at Drugs Control Department, GNCT Delhi.
Session Educator: Dr. Deepak Haldankar, Pharma manufacturing expert with 40+ years of success in managing quality for formulations and APIs, COO at H&H Healthcare and Cosmetics Pvt. Ltd.
Panel Discussion:
Shri Amit Duggal, Assistant Commissioner Drugs, FDA Punjab.
Dr. Sanjit Singh Lamba,Managing Partner, Trillyum Consulting.
- Dr. Deepak Haldankar, Pharma manufacturing expert with 40+ years of success in managing quality for formulations and APIs, COO at H&H Healthcare and Cosmetics Pvt. Ltd.
Date: 13th April | Sunday 10:30 AM IST
Session Educator: Mr. Vishal Sharma,Subject Matter Expert Co-Founder-Vi’eNnI Training & Consulting LLP
Panel Discussion:
Mr. Vishal Sharma, Subject Matter Expert Co-Founder-Vi’eNnI Training & Consulting LLP
- Ms. Ivy Louis, Subject Matter Expert, Founder – Vi’eNnI Training & Consulting LLP
- Dr. Sanjeet Singh Lamba, Managing Partner, Trillyum Consulting
Date: 6th April | Sunday 10:30 AM IST
Chief Guest: Dr. Birendra Singh, President & Global Quality Head Mankind Pharma Ltd.
Session Educator: Ms. Ivy Louis, Subject Matter Expert, Founder – Vi’eNnI Training & Consulting LLP
Panel Discussion:
Mr. Vishal Sharma, Subject Matter Expert Co-Founder-Vi’eNnI Training & Consulting LLP
Mr. Dhaval Surti, Technical Lead, Nivagen Pharmaceuticals, USA
- Ms. Ivy Louis, Subject Matter Expert, Founder – Vi’eNnI Training & Consulting LLP
Date: 16th March | Sunday 10:30 AM IST
Chief Guest: Dr. Chandrashekar Ranga, Joint Drugs Controller (I) CDSCO
Session Educator: Dr. Sanjit Singh Lamba, Managing Partner, Trillyum Consulting
Date: 2nd March | Sunday 10:30 AM IST
Chief Guest: Dr. Viranchi Shah, Spokesperson – IDMA, COA Member – pharmexcil, Promotor & Director – Saga Lifesciences Limited
Session Educator: Mr. Abhijit S. Kulkarni, VP CQA (Global Compliance & Biotech CQA) – Lupin.
Panel Discussion:
Mr. A V Jayakumar, President- Quality, Ajanta Pharma Limited.
Dr. Udaykumar Rakibe, Pharmaceutical Quality Management Expert, Formerly at Wockhardt, Intas, Ranbaxy etc. Founder – PharmaMantraTM.
- Mr. Abhijit S. Kulkarni, VP CQA (Global Compliance & Biotech CQA) – Lupin.
Date: 16th Feb | Sunday 10:30 AM IST
Chief Guest: Mr. Tajber Singh, Drug Controller, Uttarakhand.
Session Educator: Mr. Rajendra Dadhich,Senior Vice President – Corporate Quality at IPCA.
Panel Discussion:
Dr. Deepak Haldankar, Pharma manufacturing expert with 40+ years of success in managing quality for formulations and APIs.
Dr. Sanjit Singh Lamba, Managing Partner, Trillyum Consulting.
- Mr. Rajendra Dadhich,Senior Vice President – Corporate Quality at IPCA.
Date: 2nd Feb | Sunday 10:30 AM IST
Chief Guest: Mr. Sudarshan Jain, Secretary General, Indian Pharmaceutical Alliance (IPA), Former MD, Abbott Healthcare.
Session Educator: Ms. Balwinder Kaur, Pharmaceutical Quality Consultant, 35+ years in Quality function
Panel Discussion:
Dr. Jitender Khurana, International GMP Consultant: Quality System, Auditing, FDA Remediation and Training.
Dr. Sanjit Singh Lamba, Managing Partner, Trillyum Consulting.
- Ms. Balwinder Kaur, Pharmaceutical Quality Consultant, 35+ years in Quality function.
Date: 5th Jan | Sunday 10:30 AM IST
Chief Guest: Mr. Raja Bhanu,Director General of Pharmexcil.
Session Educator: Dr. Hargovind Seth, Head-QC, Windlas Biotech Ltd.
Panel Discussion:
Ms. Balwinder Kaur, Pharmaceutical Quality Consultant, 35+ years in Quality function.
Mr. Dinesh Mehandale,Assistant Vice President QA, Relicare Tech Services Pvt. Ltd
- Dr. Hargovind Seth, Head-QC, Windlas Biotech Ltd.
Date: 29th Dec | Sunday 10:30 AM IST
Chief Guest: Mr. Anil Matai, Director General, OPPI India.
Session Educator: Mr. A V Jayakumar,President- Quality, Ajanta Pharma Limited.
Panel Discussion:
Dr. Jitender Khurana, International GMP Consultant: Quality System, Auditing, FDA Remediation and Training.
Dr. Sanjit Singh Lamba,Managing Partner, Trillyum Consulting.
- Mr. A V Jayakumar,President- Quality, Ajanta Pharma Limited.
Date: 15 Dec | Sunday 10:30 AM IST
Chief Guest: Dr. Y K Gupta, President AIIMS Jammu, Principal Adviser, GARDP (Global Antibiotic Research and Development Partnership).
Session Educator: Dr. Deo Narain Dikshit, Director at AQEX Phamasolutions Pvt. Ltd., Former Vice President and Regional Quality Head Asia in Sun Pharma.
Panel Discussion:
Dr. Jitender Khurana, International GMP Consultant: Quality System, Auditing, FDA Remediation and Training.
Mr. Subhrangshu Chaudhury, Vice President & Head of Quality at Centaur Pharmaceuticals Pvt. Ltd.
- Dr. Deo Narain Dikshit,Director at AQEX Phamasolutions Pvt. Ltd., Former Vice President and Regional Quality Head Asia in Sun Pharma.
Date: 1st Dec | Sunday 10:30 AM IST
Chief Guest: Dr. Ashok Bhattacharya, Global Health & Pharma Consultant, Former Executive Director, Takeda India
Session Educator: Dr. Govind Pandey, CEO & Managing Director, Gamp Technologies Pvt Ltd & Director of Kopran Limited.
Panel Discussion:
Dr. Deepak Haldankar, Pharma manufacturing expert with 40+ years of success in managing quality for formulations and APIs.
Mr. Subhrangshu Chaudhury, Vice President & Head of Quality at Centaur Pharmaceuticals Pvt. Ltd.
- Dr. Govind Pandey, CEO & Managing Director, Gamp Technologies Pvt Ltd & Director of Kopran Limited.
Date: 24th Nov | Sunday 10:30 AM IST
Chief Guest: Shri Bodh Raj Sikri, Chairman – FOPE
Session Educator: Dr. Vineet Bhushan,Certified IRCA PQMS-GMP Auditor, Founder & CEO – Stellar Pharma Solutions.
Panel Discussion:
Mr. Vishal Sharma,Co-founder at Vi’eNnI TRAINING & CONSULTING LLP.
Dr. Sanjit Singh Lamba, Managing Partner, Trillyum Consulting.
- Dr. Vineet Bhushan,Certified IRCA PQMS-GMP Auditor, Founder & CEO – Stellar Pharma Solutions.
Date: 10th Nov | Sunday 10:30 AM IST
“Good Documentation Practices as per Revised Schedule M” will provide insights into the essential documentation protocols for the pharma industry. Learn how to maintain accuracy, consistency, and compliance with the latest standards. Elevate your documentation skills to meet regulatory expectations with ease.
Chief Guest: Shri Shobhit Koshta, Deputy Drugs Controller & Licensing Authority, Food and Drug Administration, Madhya Pradesh
Session Educator: Mr. Vijay Kshirsagar, 38+ years of experience as Quality, Regulatory & Analytical professional in reputed Pharma firms, Director & CEO at TRAC Pharma Consulting
Panel Discussion:
Dr. Damodharan Muniyandi, Chief Quality Officer – Global Quality & Regulatory AffairsSai Life Sciences Ltd.
Dr. L. Ramanathan, Associate Vice President – Technical, Apex Laboratories Pvt. Ltd. VP- Tamilnadu PMA, Jt. Sec- CiPi, EC Member- FOPE
- Mr. Vijay Kshirsagar, Director & CEO at TRAC Pharma Consulting
- Mr. Harish K Jain, President FOPE, Director Embiotic Laboratories
Date: 20th Oct | Sunday 10:30 AM IST
Join us for an insightful session on “Personal Hygiene, Sanitation & Contamination Control” where you’ll gain essential knowledge aligned with the Revised Schedule M guidelines.
This session will cover key practices to ensure cleanliness, control contamination, and maintain personnel hygiene in pharmaceutical manufacturing. A must-to-attend for anyone looking to enhance their understanding of these critical aspects of quality management.
Chief Guest: Dr. S V Veeramani, Chairman, Pharmexcil, CMD, Fourrts (India) Laboratories Pvt Ltd
Session Educator: Mr. Karan Rajendra Khairnar,Sr. Global Technical Manager at Ecolab Life Science, IRCA GMPPQS Lead Auditor, PCQI, Lean Six Sigma Black Belt (ASQ)
Panel Discussion:
Mr. Dr. Vineet Bhushan, Certified IRCA PQMS-GMP Auditor, Founder & CEO – Stellar Pharma Solutions
Mr. Harish K Jain, President FOPE, Director Embiotic Laboratories
- Dr. Sanjit Singh Lamba, Managing Partner, Trillyum Consulting
- Mr. Chakravarthi AVPS, Chairman (TG & AP), FOPE, Honorary Advisor – Pharmaceutical Export ProMotion Council, Govt of India
Vote of Thanks:
- Mr. Amit Chawla, Director – McW Healthcare
Date: 6th Oct | Sunday 10:30 AM IST
Chief Guest: Thiru. M. N. Sridhar, Joint Director of Drugs Control cum Controlling Authority (i/c), State Licensing & Controlling Authority – Tamilnadu (Allopathy, Homeopathy & Approved Drugs).
Session Educator: Mr. Manish Bhatkar, Subject Matter Expert – Aseptic Processing, Founder & CEO at RedLotus Pharmtech Private Limited.
Panel Discussion:
Mr. T. K. Raghuraman, DGM Quality at Apex Laboratories Pvt. Ltd.
Dr. Sanjit Singh Lamba, Managing Partner, Trillyum Consulting
Date: 22nd Sept | Sunday 10:00 AM IST
Chief Guest: Dr. Manish Kapoor, State Drugs Controller of Himachal Pradesh.
Session Educator: Mr. Shoeb Kurawadwala , Founder & Managing Director at CN Water, Subject Matter Expert on Water for Pharmaceutical Purposes.
Panel Discussion:
Mr. Rajesh Madan, CEO, Medicamen Biotech Limited.
Mr. Manojkumar Singh, Founder / Director of Maanvi Ecotech, Ultrapure Water Expert with 24 Years of Experience.
Date: 8th Sept | Sunday 10:30 AM IST
Understand the critical processes of qualification and validation in pharmaceutical manufacturing. This session will cover essential strategies to ensure equipment, systems, and processes consistently produce quality products meeting regulatory standards.
Chief Guest: Dr. Hemant G. Koshia, Commissioner – Food and Drugs Control Administration, Gujarat.
Session Educator: Dr. Sanjit Singh Lamba, Managing Partner, Trillyum Consulting
Panel Discussion:
Dr. Subhash Pande, Principal Adviser – Projects, cGMP compliance, Regulatory Inspections and Training, Ex Lupin, Glenmark, Zydus Cadila.
Dr. Sanjit Singh Lamba, Managing Partner, Trillyum Consulting
Mr. Vinod Kalani, Co-chairman FOPE, President RPMA, Advisor CIPI , EC Member IDMA, Cris Pharma India Ltd, Oasis I tech Ltd.
11th Aug, Sunday 10:30 AM – 12:30 PM IST
Understand the principles and processes of Quality Risk Management (QRM) in the pharmaceutical industry. This session will guide you through identifying, assessing, and controlling risks to enhance product quality and ensure regulatory compliance.
Chief Guest: Shri. Manmohan Taneja, State Drugs Controller & Licensing Authority, FDA, Haryana.
Session Educator: Dr. Udaykumar Rakibe, Pharmaceutical Quality Management Expert, Formerly at Wockhardt, Intas, Ranbaxy, Gland, Dabur, Ranbaxy, GSK, Founder – PharmaMantraTM.
Panel Discussion:
Dr. Bhaskaran. J, Deputy Drugs Controller, Regional Office, Bengaluru.
Dr. Rajiv Desai, Senior Technical Advisor, Quality and Regulatory with
Indian Pharmaceutical Alliance (IPA).Ms. Mala Sivaramakrishnan, Director – Head, Site quality
CIPLADr. Udaykumar Rakibe, Pharmaceutical Quality Management Expert, Formerly at Wockhardt, Intas, Ranbaxy, Gland, Dabur, Ranbaxy, GSK, Founder – PharmaMantraTM.
28th July, Sunday 10:30 AM – 12:30 PM IST
Explore the essential components of Pharma Quality Systems and their critical role in ensuring product quality and regulatory compliance. This session will provide insights into effective PQS implementation and maintenance, helping you enhance your organization’s quality management practices.
Chief Guest: Dr. Umesh S, Additional Drugs Controller Karnataka.
Session Educator: Dr. Ranjit Barshikar, CEO – QbD / cGMP Consulting (Biopharma, Pharma, AI- Pharma 4.0), 100-Most Impactful Healthcare Global Leader, Quality Adviser – United Nations MPP Geneva. “Quality Champion GOLD” award by Govt. Of India.
Panel Discussion:
Mr. P Ramesh, Deputy Drugs Controller (Hq), Karnataka.
Dr. Vinay Nayak, Independent Director at Aarti Pharmalabs Limited, Former President – Alembic Pharmaceuticals. Pharma India Ltd, Oasis I tech Ltd.
Dr. Ranjit Barshikar, CEO – QbD / cGMP Consulting (Biopharma, Pharma, AI- Pharma 4.0), 100-Most Impactful Healthcare Global Leader, Quality Adviser – United Nations MPP Geneva. “Quality Champion GOLD” award by Govt. Of India.
Mr. Ajay Mallesha, Quality Assurance Manager, AstraZeneca – Maryland, USA.
14th July, Sunday 11:00 AM IST
Gain a comprehensive understanding of the key changes in the revised Schedule M and learn how to develop a practical implementation plan to meet the new GMP standards. This session will equip you with the knowledge to ensure your processes are compliant and optimized for quality and safety.
Chief Guest: Dr. Chandrashekar Ranga, Joint Drugs Controller (I) CDSCO
Session Educator: Dr. Sanjit Singh Lamba, Managing Partner – Trillyum Consulting
Panel Discussion:
- Dr. Chandrashekar Ranga, Joint Drugs Controller (I) CDSCO
- Mr. Vinod Kalani, Co-chairman FOPE, President RPMA, Advisor CIPI, EC Member IDMA, Cris Pharma India Ltd, Oasis I tech Ltd.
- Dr. Rajesh Gupta, All India Pharma Committee Head of Laghu Udyog Bharati & President Himachal Drug Manufacturers Association BADDI, Co-Chairman – FOPE
- Dr. Sanjit Singh Lamba, Managing Partner – Trillyum Consulting
Date: To be updated | Sunday 10:30 AM IST
Date: To be updated | Sunday 10:30 AM IST
Will I get the certificate?
The certificate will be provided as per the following criteria.
- If you are booking a seat for a particular session, you will get the certificate for that session only.
- If you are booking the full-year package then you will get the certificates of each session as well as a special separate certificate for the overall full-year program.
Event Policy
Please note, once the payment has been made, no money will be refunded or exchanged for another type of service as compensation.
- This is to inform that recording will be available as course only to the participants who pay for the full-year package.
- The recording will be converted to course after the session and access will be provided to the paid participants of the full-year package.
- Also, you are not allowed to record and keep a copy of such resources in any manner.
Only those who book a seat and attend the session shall be eligible to receive a certificate. Please note, that a separate certificate will be provided for each session.
IMPORTANT: A special certificate for professionals who attend all the sessions.
Email: info@pharmastate.com
WhatsApp (Text only): +91-8587874143
Click here to connect directly at WhatsApp
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Don’t miss this opportunity to stay ahead of the curve and ensure your Pharma Manufacturing & Quality Practices are compliant with the latest Revised Schedule M Guidelines.
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