Experience

INTERNATIONAL INSTITUTE OF BIOTECHNOLOGY AND TOXICOLOGY
• India
• Research Services
• 1 - 100 Employee
• Senior Scientist

  • Nov 2022 - Present


Vanta Bioscience Limited

• India
• Research
• 1 - 100 Employee

• Senior Manager Toxicology

  • Apr 2017 - Present

  In Charge of General Toxicology Study Director for General and Reproduction Toxicity Studies In Charge of General Toxicology Study Director for General and Reproduction Toxicity Studies



Indigene Pharmaceuticals

• India
• Biotechnology Research

• Manager medical Affairs ( preclinical and clinical )

  • Oct 2007 - Present

  I am presently working as a Manager (Toxicology) with Indigene Pharmaceuticals, Hyderabad from October, 2007 with the Medical Affairs Department. In my line of work, I have to closely interact with the regulatory, medical affairs, data management and Pharmacovigilance wing. I have developed a close understanding of the roles and responsibilities of these departments and how to integrate their functions and work as a team. I am presently working as a Manager (Toxicology) with Indigene Pharmaceuticals, Hyderabad from October, 2007 with the Medical Affairs Department. In my line of work, I have to closely interact with the regulatory, medical affairs, data management and Pharmacovigilance wing. I have developed a close understanding of the roles and responsibilities of these departments and how to integrate their functions and work as a team.



Vanta Bioscience (A Division of Industries South Asia Private Limited)

• Associate Scientist-III

  • Jul 2012 - Mar 2017

  In Charge of General ToxicologyStudy Director for General and Reproduction Toxicity Studies

• Associate Scientist-III

  • Jul 2012 - Mar 2017

  In Charge of General ToxicologyStudy Director for General and Reproduction Toxicity Studies



Dr. Reddy's Laboratories

• India
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Assistant Manager (Preclinical )

  • Dec 2005 - Oct 2007

  Work activities include: •Developing and writing toxicology protocols •Data collection from various CRO •Reports checking and complying schedule ‘Y” Guidelines •Managing regulatory authority applications and approvals, who oversee the research and marketing of new and existing drugs •Approval for DCGI for various Drugs •Preparing final reports and conclusion for non-clinical studies Regulatory Affairs: •Provide regulatory advice as needed to the Non - Clinical Support Office relating to GLP. •Provide general regulatory advice as needed Show less



Jai Research foundation

• India
• 1 - 100 Employee

• Research officer

  • Apr 1998 - Nov 2005

  Acute Studies: •Acute Oral Toxicity in Rat. •Acute Oral Toxicity in Mice. •Acute Dermal Toxicity in Rat. •Acute Dermal Toxicity in Rabbit. •Vaginal Mucous Membrane Irritation in Rabbit. •Primary Skin Irritation in Rabbit. •Skin Sensitization in Guinea pig, •Synergism.Potentiation in Rat. Reproduction Toxicology: •Teratology/prenatal Study (Rodent and Non-rodent). •One Generation Reproduction Toxicity study in rat. •Two-Generation Reproduction Toxicity study in rat •Sperm analysis for reproduction studies. Sub Chronic 28-day oral toxicity study in Rat. 21/28 Dermal toxicity studies in Rat. 21/28 Dermal toxicity studies in Rabbit. Responsibilities in the Organization SOP preparation and implementation as per OECD,EC and CIB Protocol preparation Show less