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International Safety Systems, Inc. 
Due Diligence Audits at Pharmaceutical 
contract Manufacturing Sites in India - Lessons 
Learned 
Prasanth.K, Deputy Project Manager, India 
Pinky Bhatt, Project Manager, Asia-Pacific 
International Safety Systems, Inc. (ISS), India 
www.issehs.com
AGENDA 
 Pharmaceutical growth in India 
 EHS status at Contract Manufacturing 
sites 
 EHS audit objectives and methods 
 Observations 
 Outcomes 
 Lessons Learned 
www.issehs.com
EVOLUTION OF INDIAN PHARMA INDUSTRY
India – Major focus for Contract 
Manufacturing 
According to a study in 2013, India is: 
 4th in the world in terms of production volumes 
 13th in domestic consumption 
 Over 55% exports of India are to highly 
regulated markets 
 Largest exporter of formulations in terms of 
volume with 14 % market share 
www.issehs.com
Contract Manufacturing Sites- 
EHS Status 
 Expert in manufacturing APIs and Formulations 
 Limited EHS resources 
– Competent professionals with competency in IH and 
Process safety 
– Understanding of IH significance especially for high 
potent compounds 
– Trained mentors such CIHs 
 Willingness to learn and change 
 Safety and environmental compliance is little 
better – IH Process Safety needs significant 
improvements 
www.issehs.com
EHS Audits 
 Due Diligence audits for 
– Potential suppliers 
– With QA/QC Team 
 EHS Assessments for 
– Existing Suppliers 
– API Manufacturing sites 
– Formulation sites 
– Vaccine plant 
www.issehs.com
EHS Audits Conducted 
 India: 
– Tarapur, Hyderabad, Goa, Mumbai, 
Visakhapatanam, Ahmedabad, 
Solapur, Cuddalore, Chennai, 
Renukoot, more cities 
 China (Two sites) 
 Thailand (One site) 
 Malaysia (One site) 
 Indonesia (One site) 
 Egypt (One site) 
www.issehs.com
EHS Audits Conducted 
 Germany 
– Leverkusen 
– Dessau-Wörlitz 
 Ireland 
– Arklow 
 France 
– Calais 
 Spain 
– Barcelona 
 Ukrain 
 Hungary (Budapest) 
www.issehs.com
EHS Audits Conducted 
 USA 
– Rancho Cordova, CA 
– North Bend, LA 
– Hickok, KS 
 Canada 
– Hamilton 
 Brazil (two sites) 
www.issehs.com
EHS Audit Objectives 
 Evaluate compliance status with local health 
safety and environmental regulations 
 Evaluate site status with Pharmaceutical Supply 
Chain Initiative, 
http://pharmaceuticalsupplychain.org/ 
 Evaluate site status on generally accepted 
industry practices for EHS 
www.issehs.com
EHS Elements Covered 
 EHS organization and staffing, Employee EHS training 
 Air Emissions, Wastewater Management, Waste 
Management, Spill Prevention 
 Hazard Assessment, Risk Assessment and Industrial 
Hygiene Program 
 Process Safety Management 
 Emergency Response and Planning 
 Personal Protective equipment -Written programs, Cleaning 
and decontamination, Gowning de-gowning 
www.issehs.com
EHS organization and staffing 
 EHS Staffing and Competencies 
 Health, Safety, Environment Policy 
 Safety committees 
 Accidents reporting and investigation 
 Training matrices and training conducted 
www.issehs.com
Air Emissions, Wastewater Management, 
Waste Management, Spill Prevention 
 License to operate 
 Permits 
 Pollution control 
 Waste water treatment, Water discharge, 
sampling, sludge solid handling 
 Liquid and solid waste handling 
 Used container, packing material handling and 
disposal 
 Hazardous waste handling and disposal 
www.issehs.com
Risk Assessment and Controls 
 Hazard Communication, Chemical Inventory, 
Labeling, MSDS 
 Risk Assessment procedures, Follow up 
 Qualitative and quantitative exposure assessment 
 Potent compound handling /Particulate 
containment 
 Hierarchy of exposure control measures and 
validation 
 Equipment and personnel entry and exit 
 Local Exhaust Ventilation and Preventive 
Maintenance 
www.issehs.com
General Safety and Controls 
 Job Safety Analysis 
 Permit Systems 
 Fall Protection 
 Machine Guarding 
 Electrical safety and energy isolation procedures 
 Housekeeping 
www.issehs.com
Process Safety 
 Storage, handling and transportation of 
flammable and reactive chemicals 
 Storage tanks 
 Pressure vessels 
 Safety valves 
 Control of ignition sources (e.g., static 
electricity) in flammable area 
 Inerting, validation of inerting 
 Compressed gases, boiler and pressure vessels 
controls 
www.issehs.com
Life Safety and Emergency 
Response 
 Means of egress 
 Fire Protection Systems and Alarms 
 Written Plans 
 Evacuation Procedures 
www.issehs.com
Evaluation Criteria 
 Parent company specific guidelines 
 Local regulations 
 National and international standards 
 Best Practices in pharmaceutical industries 
www.issehs.com
Audit Process followed 
 Planning 
– EHS Questionnaire 
 Site visit (3 to 5 days) 
– Opening meeting /introduction 
– Walkthrough 
– Detailed site visit 
– Stake-holders meeting (maintenance, Engineering, 
Physician) 
– Documents review 
– Closing conference 
Draft and final report 
www.issehs.com
Most Common Observations- 
Environment 
 Regulatory 
– Environment Consent Requirements (quantity 
of waste generated, disposed off) 
 Non-regulatory 
– Determining presence of API in Waste 
www.issehs.com
Most Common Observations- 
Process safety and personal 
safety 
 Process Safety 
– Nitrogen inerting not done at all or not validated 
– Grounding/Bonding and static electricity control 
measures 
– Flammable tank/container storage (Dike capacity, 
flame arrestor) 
 Personal Safety 
– Energy Isolation procedures 
– Fall Protection 
www.issehs.com
Most Common Observations- 
Industrial Hygiene 
 Qualitative Exposure Assessment 
 Reliable, reproducible and representative 
quantitative exposure assessment for APIs and 
solvent 
 Hierarchy of Controls (RPE reliance) 
 Robust RPE program 
 Gowning de-gowning, airlock rooms 
 Potential contamination of Green Zones 
www.issehs.com
Outcome 
 Sites receptive and supportive 
 Some of the observations addressed immediately 
 After audits, QLEA and QNEA were conducted with 
reliable methods 
 Containment validation conducted as required from 
parent company 
 Significant increase in awareness for IH and Process 
Safety 
 Basic training conducted 
www.issehs.com
Lessons Learned 
 Auditing – especially based on site visit to 
determine effectiveness of compliance – is 
powerful tool in ensuring EHS compliance status 
and reducing EHS risk 
 Spend more at site at every corner and less in 
looking at records 
 Closing meeting – to receive feedback before 
report goes out is critical 
 Stay away from commenting audit conclusions 
such as “show stoppers” until all aspects are 
considered 
www.issehs.com
Thank You 
Questions?? 
25

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Due Diligence Audit By Pinky Bhatt & Prashant Kondragunta, ISS

  • 1. International Safety Systems, Inc. Due Diligence Audits at Pharmaceutical contract Manufacturing Sites in India - Lessons Learned Prasanth.K, Deputy Project Manager, India Pinky Bhatt, Project Manager, Asia-Pacific International Safety Systems, Inc. (ISS), India www.issehs.com
  • 2. AGENDA  Pharmaceutical growth in India  EHS status at Contract Manufacturing sites  EHS audit objectives and methods  Observations  Outcomes  Lessons Learned www.issehs.com
  • 3. EVOLUTION OF INDIAN PHARMA INDUSTRY
  • 4. India – Major focus for Contract Manufacturing According to a study in 2013, India is:  4th in the world in terms of production volumes  13th in domestic consumption  Over 55% exports of India are to highly regulated markets  Largest exporter of formulations in terms of volume with 14 % market share www.issehs.com
  • 5. Contract Manufacturing Sites- EHS Status  Expert in manufacturing APIs and Formulations  Limited EHS resources – Competent professionals with competency in IH and Process safety – Understanding of IH significance especially for high potent compounds – Trained mentors such CIHs  Willingness to learn and change  Safety and environmental compliance is little better – IH Process Safety needs significant improvements www.issehs.com
  • 6. EHS Audits  Due Diligence audits for – Potential suppliers – With QA/QC Team  EHS Assessments for – Existing Suppliers – API Manufacturing sites – Formulation sites – Vaccine plant www.issehs.com
  • 7. EHS Audits Conducted  India: – Tarapur, Hyderabad, Goa, Mumbai, Visakhapatanam, Ahmedabad, Solapur, Cuddalore, Chennai, Renukoot, more cities  China (Two sites)  Thailand (One site)  Malaysia (One site)  Indonesia (One site)  Egypt (One site) www.issehs.com
  • 8. EHS Audits Conducted  Germany – Leverkusen – Dessau-Wörlitz  Ireland – Arklow  France – Calais  Spain – Barcelona  Ukrain  Hungary (Budapest) www.issehs.com
  • 9. EHS Audits Conducted  USA – Rancho Cordova, CA – North Bend, LA – Hickok, KS  Canada – Hamilton  Brazil (two sites) www.issehs.com
  • 10. EHS Audit Objectives  Evaluate compliance status with local health safety and environmental regulations  Evaluate site status with Pharmaceutical Supply Chain Initiative, http://pharmaceuticalsupplychain.org/  Evaluate site status on generally accepted industry practices for EHS www.issehs.com
  • 11. EHS Elements Covered  EHS organization and staffing, Employee EHS training  Air Emissions, Wastewater Management, Waste Management, Spill Prevention  Hazard Assessment, Risk Assessment and Industrial Hygiene Program  Process Safety Management  Emergency Response and Planning  Personal Protective equipment -Written programs, Cleaning and decontamination, Gowning de-gowning www.issehs.com
  • 12. EHS organization and staffing  EHS Staffing and Competencies  Health, Safety, Environment Policy  Safety committees  Accidents reporting and investigation  Training matrices and training conducted www.issehs.com
  • 13. Air Emissions, Wastewater Management, Waste Management, Spill Prevention  License to operate  Permits  Pollution control  Waste water treatment, Water discharge, sampling, sludge solid handling  Liquid and solid waste handling  Used container, packing material handling and disposal  Hazardous waste handling and disposal www.issehs.com
  • 14. Risk Assessment and Controls  Hazard Communication, Chemical Inventory, Labeling, MSDS  Risk Assessment procedures, Follow up  Qualitative and quantitative exposure assessment  Potent compound handling /Particulate containment  Hierarchy of exposure control measures and validation  Equipment and personnel entry and exit  Local Exhaust Ventilation and Preventive Maintenance www.issehs.com
  • 15. General Safety and Controls  Job Safety Analysis  Permit Systems  Fall Protection  Machine Guarding  Electrical safety and energy isolation procedures  Housekeeping www.issehs.com
  • 16. Process Safety  Storage, handling and transportation of flammable and reactive chemicals  Storage tanks  Pressure vessels  Safety valves  Control of ignition sources (e.g., static electricity) in flammable area  Inerting, validation of inerting  Compressed gases, boiler and pressure vessels controls www.issehs.com
  • 17. Life Safety and Emergency Response  Means of egress  Fire Protection Systems and Alarms  Written Plans  Evacuation Procedures www.issehs.com
  • 18. Evaluation Criteria  Parent company specific guidelines  Local regulations  National and international standards  Best Practices in pharmaceutical industries www.issehs.com
  • 19. Audit Process followed  Planning – EHS Questionnaire  Site visit (3 to 5 days) – Opening meeting /introduction – Walkthrough – Detailed site visit – Stake-holders meeting (maintenance, Engineering, Physician) – Documents review – Closing conference Draft and final report www.issehs.com
  • 20. Most Common Observations- Environment  Regulatory – Environment Consent Requirements (quantity of waste generated, disposed off)  Non-regulatory – Determining presence of API in Waste www.issehs.com
  • 21. Most Common Observations- Process safety and personal safety  Process Safety – Nitrogen inerting not done at all or not validated – Grounding/Bonding and static electricity control measures – Flammable tank/container storage (Dike capacity, flame arrestor)  Personal Safety – Energy Isolation procedures – Fall Protection www.issehs.com
  • 22. Most Common Observations- Industrial Hygiene  Qualitative Exposure Assessment  Reliable, reproducible and representative quantitative exposure assessment for APIs and solvent  Hierarchy of Controls (RPE reliance)  Robust RPE program  Gowning de-gowning, airlock rooms  Potential contamination of Green Zones www.issehs.com
  • 23. Outcome  Sites receptive and supportive  Some of the observations addressed immediately  After audits, QLEA and QNEA were conducted with reliable methods  Containment validation conducted as required from parent company  Significant increase in awareness for IH and Process Safety  Basic training conducted www.issehs.com
  • 24. Lessons Learned  Auditing – especially based on site visit to determine effectiveness of compliance – is powerful tool in ensuring EHS compliance status and reducing EHS risk  Spend more at site at every corner and less in looking at records  Closing meeting – to receive feedback before report goes out is critical  Stay away from commenting audit conclusions such as “show stoppers” until all aspects are considered www.issehs.com

Notes de l'éditeur

  1. India has over 550 manufacturing sites registered with the US Food and Drug Administration, of which 323 are USFDA approved, as on March 2013, says the Indian Commerce Ministry, citing Pharmaceuticals Export Promotion Council of India (Pharmexcil) data. And there are 350 manufacturing sites endorsed by the European Union for their Good Manufacturing Practices in India, as on April 2013, it added.
  2. The EHS Assessments (audits) are mostly conducted along with the QA/QC teams for potential suppliers. The assessments were also carried out for existing suppliers for APIs and formulations including vaccine mfg. plants. Formulations include tablets (coated, uncoated), capsules, liquid orals, ointments, gels