Food and Drugs Administration, (FDA) Haryana, India. |
Email ID: dahiya19@yahoo.com
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Last Updated on November 13, 2023 by The Health Master
PowerPoint Slide Show
A PowerPoint slide show is a powerful tool to use during seminars or webinars. Many PowerPoint slide shows have been presented at various events for regulatory officers and industries (pharmaceuticals, homoeopathy, cosmetics, medical devices, blood banks / centers, etc.).
These PowerPoint slide shows are very useful for the stake holders engaged in the regulatory affairs, pharma industry and health sector.
We have provided the following PowerPoint slide shows in pdf format: Click the below links to read or download:
Quality and Regulatory Compliances
“Quality and Regulatory Compliances” presented by Dr. P. V. APPAJI, M.Pharm PhD, Former Director, NPPA, Govt of India, Former Director General, PHARMEXCIL, Govt of India.
Quality and Regulatory Compliances
Medical Devices Rules 2017
“Medical Devices Rules, 2017” presented by Lalit Kumar Goel, Deputy State Drugs Controller, FDA Haryana on 13-05-2023 at Shrinagar, J&K organised by Drugs Control Officers (I) Welfare Association (DCOIWA).
Investigational Skills for Counterfeit Drugs
“Investigational Skills for Counterfeit Drugs” presented by Omprakash Sadhwani, Former Joint Commissioner & Drugs Controller, FDA Maharashtra on 13-05-2023 at Srinagar, J&K organised by Drugs Control Officers (I) Welfare Association (DCOIWA).
Investigational Skills for Counterfeit Drugs
Power of Inspectors & Sampling procedure
“Power of Inspectors & Sampling procedure” presented by Lalit Kumar Goel, Deputy State Drugs Controller, FDA Haryana on 13-05-2023 at Shrinagar, J&K organised by Drugs Control Officers (I) Welfare Association (DCOIWA).
Power of Inspectors & Sampling procedure
Inspection and Blood Centre
“Inspection and Blood Centre” Inspection and Blood Centre” presented by Lalit Kumar Goel, Deputy State Drugs Controller, FDA Haryana on 13-05-2023 at Shrinagar, J&K organised by Drugs Control Officers (I) Welfare Association (DCOIWA).
Method of investigation of NSQ and Spurious drugs
“Method of investigation of NSQ and Spurious drugs” presented by K R Chawla
Controlling Authority / Deputy Drugs Controller / Head of the Office, Drugs Control Department, Govt. of N.C.T. of Delhi on 16-02-2023 at NIHFW, Delhi
Method-of-investigation-of-NSQ-and-Spurious-drugs
Cosmetics Rules 2020
“Cosmetics Rules 2020” presented by Lalit Kumar Goel, Deputy State Drugs Controller, FDA Haryana on 04-02-2023 at Sonepat, Haryana organised by Cosmetics Chapter of Haryana Pharmaceuticals Manufacturers Association (HPMA).
FDA Inspection Overview
“FDA Inspection Overview” presented by Dr. Prabhakar Reddy Veerareddy M.Pharm., Ph.D., PDF (USA), LLB, Head University College of Pharmaceutical Sciences Palamuru University, Mahabubagar, Telangana Central Council Member-Pharmacy Council of India Secretary-IPGA, Telangana State President-Telangana Registered Pharmacist Association on 29-01-2023 at Hyderabad, organised by Drugs Control Officers (I) Welfare Association (DCOIWA).
Medicine in India: Affordability and Accessibility Challenges
“Medicine in India: Affordability and Accessibility Challenges”, presented by A. Mangakandan, M.Pharm, Ph.D., IAS, Chief Development Officer, Agra, UP, India, at the 72nd International Pharmaceutical Congress on January 20–22, 2023, in Nagpur, Maharashtra.
Medical Devices Rules, 2017
“Medical Devices Rules, 2017” presented by Lalit Kumar Goel, Deputy State Drugs Controller, FDA Haryana on 18-12-2022 at Agartala, Tripura organised by Drugs Control Officers (I) Welfare Association (DCOIWA).
Investigational Skills for Counterfeit Drugs
“Investigational Skills for Counterfeit Drugs” presented by Omprakash Sadhwani, Former Joint Commissioner & Drugs Controller, FDA Maharashtra on 18-12-2022 at Agartala, Tripura organised by Drugs Control Officers (I) Welfare Association (DCOIWA).
Labelling & Pack Size of Drugs
“Labeling & Pack Size of Drugs under the Drugs Act, 1940 & Rules, 1945″ presented by Lalit Kumar Goel, Deputy State Drugs Controller, FDA Haryana, on 17-12-2022 at Raipur, Chhattisgarh organised by Drugs Control Officers (I) Welfare Association (DCOIWA).
Legal drafting of documents
“Legal drafting of documents” presented by R K Harna, former Asstt. State Drugs Controller, FDA Haryana on 17-12-2022 at Raipur, Chhattisgarh organised by Drugs Control Officers (I) Welfare Association (DCOIWA).
Compiled by:
Rakesh Dahiya, SDCO cum Licensing Authority, FDA Haryana
How to Become a Skilled Manufacturing Chemist in the Pharma Industry
Sweet Science: Exploring Importance of Inverted Sugar in Pharma Industry
NABL certification for Laboratories: Let’s understand
Major FDA audit findings about Equipment and Instruments
Equipment and Instruments: Maintenance, difference and importance in the Pharma Industry
Quality Assurance in the Pharmaceutical Industry
NIPER: A Comprehensive Guide to NIPER Institutes in India
Latest on Indian Pharmacopoeia Commission (IPC)
Types of inspections done by USFDA: Read in detail
AHUs, Air Types, Air Changes and their Functions in Pharma Industry
Understanding Airlock Systems in Pharma Industry
Upcoming events: Pharma, Cosmetics, Homoeopathy & Medical Devices
Cosmetics Testing in India: A Comprehensive Guide
Airlocks in the Pharma Industry: An essential component
Line clearance and maintenance in manufacturing: A comprehensive guide
Difference between Validation and Calibration in the Pharma Industry
The Effectiveness of 70% Alcohol as a Disinfectant
Wet Granulation vs Dry Granulation: Understanding the Key Differences
Understanding GMP, cGMP, and WHO-GMP
USFDA issues Form 483 to Pharma Companies: Let’s know all about it
Calibration of Laboratory Instruments
Difference: Disintegration and Dissolution test in pharma industry
How to prepare SOPs in the Pharma Industry
Difference between branded and generic medicines
Understanding DQ, IQ, PQ, and OQ in the Pharma Industry
Duties and responsibilities of QA person in Pharma Industry
Types of Tablet Coating and its Functionality in pharma industry
Dissolution test: Importance in Pharma Industry
Lux level in Industry (Pharma, Cosmetics, Homeopathy & Medical Devices)
NSQ Drug: Route cause analysis and CAPA
Area required for manufacturing of Drugs, Cosmetics, Homoeopathic & Blood Centre
Licensing procedure for manufacturing of Drugs
Procedure to obtain license for manufacturing of Cosmetics
Procedure to obtain license for manufacturing of Homoeopathic Medicines
Procedure to obtain license for manufacturing of Medical Devices
Procedure to obtain License to Manufacture drugs for testing and analysis purposes
Procedure to obtain license for Blood Centre (Blood Bank)
Procedure to obtain license for Commercial Testing Laboratories
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