D

Dr. Ankushreddy Patil, MVSc, DABT

Associate Consultant

Bengaluru, Karnataka, India18 yrs 8 mos experience
Most Likely To SwitchHighly Stable

Key Highlights

  • Over 16 years of experience in toxicology and risk assessment.
  • DABT certified with expertise in consumer safety.
  • Specialized in regulatory compliance for cosmetics and consumer products.
Stackforce AI infers this person is a Toxicology and Risk Assessment expert in the Consumer Products and Pharmaceuticals industry.

Contact

LinkedIn

Skills

Core Skills

ToxicologyRisk AssessmentRegulatory Compliance

Other Skills

Healthcare ConsultingPharmacologyGLPDrug DevelopmentIn VivoCROLifesciencesProject ManagementClinical DevelopmentRegulatory AffairsCosmetics safetyConsumer ToxicologyREACH ComplianceMicrosoft PowerPoint

About

As a passionate and self-motivated toxicologist, I am dedicated to learning and contributing to consumer safety through the practice of Toxicology and Risk Assessment. I am a Diplomate of the American Board of Toxicology (DABT) with over 16 years of research and consulting experience. I specialise in the human health hazard and risk assessment of chemical substances and consumer products, including cosmetics and other personal care products (PCPs). I have extensive experience in safety and risk assessment as well as regulatory compliance for cosmetics and consumer products following global regulations. Additionally, I have experience in preparing critical reviews and toxicological assessments of substances in different sectors such as chemicals and pharmaceuticals, including deriving safe levels like PDEs/ADIs. Specialities: Consumer/cosmetics Toxicology, Hazard and safety assessments, Toxicological risk assessment of ingredients/products, Product Safety and stewardship, Project Management in Regulatory Toxicology

Experience

Toxminds

2 roles

Principal Consultant at ToxMinds India Consulting Pvt. Ltd

Promoted

Sep 2024 – Present · 1 yr 6 mos · Bengaluru, Karnataka, India · On-site

Senior Consultant at ToxMinds India Consulting Pvt. Ltd

Nov 2019 – Aug 2024 · 4 yrs 9 mos · Bengaluru, Karnataka, India · On-site

  • My job profile and responsibilities include:
  • Conducting systematic literature reviews for safety assessments of diverse cosmetic ingredients, encompassing chemicals, impurities, and botanicals.
  • Interpreting a wide range of scientific data and effectively communicating findings in compliance with regulatory requirements.
  • Preparing toxicological or hazard profiles for raw materials, ingredients, and impurities.
  • Performing safety assessments for various products, such as cosmetics, consumer products, natural healthcare products, detergents, and cleaning products.
  • Conducting safety assessments of raw materials and characterizing their risks based on Margin of Safety( MoS) or Margin of Exposure (MoE) calculations.
  • Conducting an independent toxicological review of the classification (CLH) proposal
  • Preparation of SCCS Notes of Guidance (NOG) compliant safety dossier for cosmetic ingredients.
  • Contributing to the evaluation of substances to identify potential endocrine-disrupting properties.
  • Preparing, reviewing, and ensuring the quality of toxicological reports for setting health-based exposure limits (HBEL) related to permitted/acceptable daily exposure (PDE/ADE) and Tolerable Daily Intake (TDI/TI) for pharmaceutical active ingredients, impurities, residuals, solvents, extractables, and leachables (E&L).
  • Determining preclinical testing requirements to support developmental projects.
  • Reviewing study plans and reports for various health/regulatory authority submissions.
  • Using and being involved in New Approach Methodologies (NAM) and Next Generation Risk Assessment (NGRA).
Healthcare ConsultingToxicologyRisk Assessment

Johnson & johnson ltd

2 roles

Principal Scientist, Toxicology Resource Centre

Promoted

Mar 2013 – Oct 2019 · 6 yrs 7 mos · Mumbai

  • My job profile included
  • Conducting safety assessments for various cosmetic ingredients and raw materials, including chemicals, botanicals, and fragrances/flavors.
  • Evaluating cosmetic products/formulations for safety and regulatory registration.
  • Preparing and reviewing Cosmetic Product Safety Reports (CPSRs).
  • Determining preclinical/clinical testing requirements to support developmental projects.
  • Engaging in toxicology research and regulatory projects.
  • Summarizing, analyzing, and interpreting test results for submission to regulatory agencies.
  • Preparing expert statements and data-waiving statements according to regulations and guidelines.
  • Managing a team of scientists for the safety evaluation of cosmetic products.
  • Providing training and reviewing assignments for team members.
ToxicologyRegulatory Compliance

Senior Scientist (Executive), Toxicology Resource Centre

May 2011 – Feb 2013 · 1 yr 9 mos · Mumbai

  • Safety assessment of cosmetic products
Toxicology

Evalueserve

Senior Research Associate - REACH & Toxicology

Aug 2009 – Apr 2011 · 1 yr 8 mos

  • My job profile and responsibilities included:
  • Conducting toxicology research and regulatory projects.
  • Preparing study summaries for physico-chemical, environmental, and human health endpoints for REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) registration dossiers.
  • Performing literature searches on hazardous effects from various databases and identifying toxic effects of various chemicals on humans, animals, aquatic life, and the environment.
  • Creating hazard assessments/toxicological profiles for chemicals and cosmetics.
  • Compiling safety assessment reports for baby care and cosmetic products.
  • Conducting QSAR analysis for data gaps and preparing reports.
  • Preparing CLP matrices and Chemical Safety Assessments/Reports for REACH submission.
  • Developing training modules on REACH.
  • Evaluating regulatory study reports scientifically and financially.
Toxicology

Advinus therapeutics pvt ltd, bangalore- a tata enterprise

2 roles

Associate Research Scientist -Toxicology Drug Development

Promoted

Jan 2008 – Jul 2009 · 1 yr 6 mos

  • Lead subacute and subchronic toxicity studies for New Chemical Entities (NCEs) as a Technical Coordinator and study director in Rodents and Non-rodents for regulatory submissions.
  • Develop and review Standard Operating Procedures (SOPs) for various laboratory procedures.
  • Prepare dossiers to meet various regulatory requirements.
  • Oversee study implementation and write comprehensive reports, including data interpretation.
ToxicologyRegulatory Compliance

Assistant Research Scientist-Toxicology

Sep 2007 – Jan 2008 · 4 mos

  • Preclinical Toxicologist-Study panning, scheduling, report preparation etc
Toxicology

Shriram institute for industrial research

Project Trainee

Mar 2007 – Sep 2007 · 6 mos · Delhi, India · On-site

  • • Conducting comprehensive toxicological studies, including project planning, design, execution, and results interpretation, focused on pharmaceuticals and medical devices in laboratory animals
Toxicology

Education

Indian Institute of Commerce and Trade, Lucknow

Master Diploma in Business Administration (MBA) — Pharma Marketing

Jan 2008 – Jan 2010

Catalyst Clinical Services Pvt. Ltd.New Delhi

Professional Diploma in Clinical Research — Clinical Research

Jan 2006 – Jan 2007

Maharashtra Animal and Fishery Sciences University

M.V.Sc — Veterinary Pharmacology and Toxicology

Jan 2004 – Jan 2006

Veterinary college, Bidar, UAS Dharwad

B.V.Sc &A.H. — Veterinary Science

Jan 1999 – Jan 2004

SSKB college

HSC (12th)

Jan 1997 – Jan 1999

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