Pragnesh Panchamvedi Email & Phone Number | Hello, my name is Pragnesh Panchamvedi. I am a Diplomate of American Board of Toxicology (DABT) and European Registered Toxicologist (ERT) with 11 years experience in diverse industrial & consulting environments. I like to get updated myself regularly with scientific & regulatory toxicology changes in the my professional field. I work to contribute towards making positive impact to work as well as safeguard public health from risk. I hold Masters Degree in Regulatory Toxicology from reputed premier- National Institute of Pharmaceutical Education and Research (NIPER), Punjab, India. Also, I am a member of the Belgian Society of Toxicology and Ecotoxicology, individual member of the EUROTOX and Regulatory Affairs Professionals Society (RAPS) USA. I have been registered & certified in the Belgian Chapter of European Register of Toxicologist (ERT). I am RAC certified (held since 2016, re-certified in 2019 & 2022) from RAPS. My Diverse Skill Sets are: • Toxicological Risk/Safety Assessment and Risk/Benefit Analysis using best available scientific studies data (in vivo, in vitro, in chemico, in silico) • Help in generation of Next Generation Risk Assessment (NGRA) using New Approach Methodologies (NAM) like (Q)SAR, in-vitro/in-chemico, read across • Regulatory Writing (Nonclinical & Clinical) • Medical devices Biocompatibility Assessment (ISO 10993) • EU REACH (chemicals) /EU BPR (biocides) /EU PPPR (pesticides) & EU CR (Cosmetics) regulations dossiers preparation including standard data exchange forms using IUCLID • Derivation/Revision of Acceptable/Permissible Daily Exposure/Tolerable Intake (ADE/PDE/TI), Occupational Exposure Limit (OEL) for pharmaceutical active ingredients, impurities, residuals and solvents, extractables & leachables • Impurities Qualification in Drug Substance (DS) / Active Pharmaceutical Ingredients (API) & Drug Products (DP) as per ICH/FDA/EMA guidelines (Q3 series and M7) • Computational toxicology • Help in evaluation of substances with potential endocrine disrupting properties (Endocrine disruptors) • Ability to interpret various types of complex regulatory as well as scientific data & to communicate clearly and concisely with detailed support as required for different industries • Responding to regulatory agencies and their designated notified bodies queries (i.e., FDA, EMA, ECHA, ESMA notified body) • Business Development and Digital Marketing (Social Media) communication strategies Disclaimer: Post and shared updates/news are my own personal views. It does not necessarily represent my company or employer views or support.

Pragnesh Panchamvedi

Hello, my name is Pragnesh Panchamvedi. I am a Diplomate of American Board of Toxicology (DABT) and...
Bengaluru, Bengaluru, India

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Pragnesh Panchamvedi’s Email pragnesh.panchamvedi@toxminds.com

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Pragnesh Panchamvedi’s Location Bengaluru, Bengaluru, India

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Pragnesh Panchamvedi’s Prior Industry Freelance | Sciformix | Intertek | Johnson And Johnson Consumer Health

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Work Experience

Toxminds

Consultant

Present

Freelance

Regulatory Toxicologist

2016-09-01 00:00:00 - 2017-10-01 00:00:00

Sciformix

Regulatory Affairs Specialist

2015-07-01 00:00:00 - 2016-09-01 00:00:00

Intertek

Toxicologist, Intertek Toxicology Assessment (Ita), Uk

2014-02-01 00:00:00 - 2015-06-01 00:00:00

Johnson And Johnson Consumer Health

Toxicology, Latin America (Latam) Region, Toxicology Resource Center, Global R & D

2013-10-01 00:00:00 - 2014-01-01 00:00:00

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FAQ About Pragnesh Panchamvedi

Pragnesh Panchamvedi is located at
Bengaluru, Bengaluru, India

Pragnesh Panchamvedi is a Hello, my name is Pragnesh Panchamvedi. I am a Diplomate of American Board of Toxicology (DABT) and European Registered Toxicologist (ERT) with 11 years experience in diverse industrial & consulting environments. I like to get updated myself regularly with scientific & regulatory toxicology changes in the my professional field. I work to contribute towards making positive impact to work as well as safeguard public health from risk. I hold Masters Degree in Regulatory Toxicology from reputed premier- National Institute of Pharmaceutical Education and Research (NIPER), Punjab, India. Also, I am a member of the Belgian Society of Toxicology and Ecotoxicology, individual member of the EUROTOX and Regulatory Affairs Professionals Society (RAPS) USA. I have been registered & certified in the Belgian Chapter of European Register of Toxicologist (ERT). I am RAC certified (held since 2016, re-certified in 2019 & 2022) from RAPS. My Diverse Skill Sets are: • Toxicological Risk/Safety Assessment and Risk/Benefit Analysis using best available scientific studies data (in vivo, in vitro, in chemico, in silico) • Help in generation of Next Generation Risk Assessment (NGRA) using New Approach Methodologies (NAM) like (Q)SAR, in-vitro/in-chemico, read across • Regulatory Writing (Nonclinical & Clinical) • Medical devices Biocompatibility Assessment (ISO 10993) • EU REACH (chemicals) /EU BPR (biocides) /EU PPPR (pesticides) & EU CR (Cosmetics) regulations dossiers preparation including standard data exchange forms using IUCLID • Derivation/Revision of Acceptable/Permissible Daily Exposure/Tolerable Intake (ADE/PDE/TI), Occupational Exposure Limit (OEL) for pharmaceutical active ingredients, impurities, residuals and solvents, extractables & leachables • Impurities Qualification in Drug Substance (DS) / Active Pharmaceutical Ingredients (API) & Drug Products (DP) as per ICH/FDA/EMA guidelines (Q3 series and M7) • Computational toxicology • Help in evaluation of substances with potential endocrine disrupting properties (Endocrine disruptors) • Ability to interpret various types of complex regulatory as well as scientific data & to communicate clearly and concisely with detailed support as required for different industries • Responding to regulatory agencies and their designated notified bodies queries (i.e., FDA, EMA, ECHA, ESMA notified body) • Business Development and Digital Marketing (Social Media) communication strategies Disclaimer: Post and shared updates/news are my own personal views. It does not necessarily represent my company or employer views or support.