Atul Bonde

Atul Bonde Email and Phone Number

Lead DQA - Clinical and Pharmacovigilance at Dr. Reddy's Laboratories @ Dr. Reddy's Laboratories
hyderābād, telangana, india
Atul Bonde's Location
Hyderabad, Telangana, India, India
Atul Bonde's Contact Details

Atul Bonde personal email

n/a
About Atul Bonde

Clinical Regulatory ComplianceGxP AuditseCTD publishings and checksVendor Qualification AuditsLearning and DevelopmentRegulatory Queries ResolutionChange control and CAPA Management

Atul Bonde's Current Company Details
Dr. Reddy's Laboratories

Dr. Reddy'S Laboratories

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Lead DQA - Clinical and Pharmacovigilance at Dr. Reddy's Laboratories
hyderābād, telangana, india
Website:
drreddys.com
Employees:
15315
Atul Bonde Work Experience Details
  • Dr. Reddy'S Laboratories
    Lead Dqa - Clinical And Pharmacovigilence
    Dr. Reddy'S Laboratories Sep 2019 - Present
  • Cipla
    Senior Manager
    Cipla Apr 2017 - Sep 2019
    Mumbai, Maharashtra, India
  • Cipla
    Reaearch Compliance Cell Leader
    Cipla Nov 2010 - Sep 2019
  • Unichem Laboratories Ltd
    Executive - Clinical Research
    Unichem Laboratories Ltd Jan 2010 - Nov 2010
  • Alkem Laboratories Ltd
    Clinical Research Associate
    Alkem Laboratories Ltd Sep 2006 - Jan 2010
    My job responsibilities include:Planning and execution of the study as per applicable regulatory guidelines, protocol and internal SOPs.To monitor the progress and performance of BE studies.Preparing study close out report.Shipment of Biological samples to Bioanalytical department and external CRO for analysis.Pharmacy:Receipt, Storage, Dispensing and Accountability of Investigational Drug Product and Maintenance of Pharmacy AreaCommunication with Sponsor regarding Investigational Drug Product receipt & discrepancy if any.Storage of Investigational drug products as per required regulatory norms.Clinical Data Management:Prepare study reports, listings, tables, graphs and other presentations of study data.Completion and review of Trial master files.Medical writing:Review and develop protocols.Review and approve Case Report Forms (CRFs).Study summery and clinical report writing.Prepare study reports, listings, tables, graphs and other presentations of study dataResponsible for researching, writing and editing several types of documents such as clinical study reports, clinical overviews & summaries of efficacy and safety, clinical trial protocols, investigator brochures, informed consent documents. Review and updating of Standard Operating Procedures (SOP's) of Medical concern in the Clinical Department.Administrative responsibilities:Mentoring trainee CRAs on monitoring, internal procedures, and query resolution.Mentoring trainee CRAs on project management procedures and policies.Handling a team of 7 CRA's.Preparing the study plan. To assess the adequacy of staff, facility before initiation of the study.Communication with sponsor, IEC, subjects and research team.Updating status of ongoing and completed projects from 7 CRA's, 1 Technician and 2 Phlebotomist's.Communication with Bioanalytical department or external CRO regarding analysis of Bio samples.
  • Siddhi Riddhi Agency
    Owner/Partner
    Siddhi Riddhi Agency Nov 2003 - Jun 2005
    Nashik
  • Kresp (Kopran Ltd)
    Professional Service Representative
    Kresp (Kopran Ltd) May 2003 - Oct 2003
    • Promote the company’s product to doctors and chemists in respected area.• Implement Company’s sale strategy to achieve sales target.• Co-ordination amongst company, stockiest, doctors and retailers.• Conducted CME meetings for high specialty doctors.• Prescription generation is main task as well as it must be honored.• Sales tour to increase the sales.• Conducted various medical camps like: -• Asthma camp.
  • Lyka Hetero Healthcare Ltd
    Professional Service Representative
    Lyka Hetero Healthcare Ltd Jul 2002 - Mar 2003
    • Promote the company’s product to doctors and chemists in respected area.• Implement Company’s sale strategy to achieve sales target.• Co-ordination amongst company, stockiest, doctors and retailers.• Conducted CME meetings for high specialty doctors.• Prescription generation is main task as well as it must be honored.• Sales tour to increase the sales.• Conducted various medical camps.
  • Protec (Div. Of Cipla)
    Marketing Executive
    Protec (Div. Of Cipla) Jun 1999 - Nov 1999
    • Promote the company’s product to doctors and chemists in respected area.• Implement Company’s sale strategy to achieve sales target.• Co-ordination amongst company, stockiest, doctors and retailers.• Conducted CME meetings for high specialty doctors.• Prescription generation is main task as well as it must be honored.• Sales tour to increase the sales.• Conducted various medical camps

Atul Bonde Skills

Medical Writing Cro Sop Clinical Trials Clinical Study Design Fda Ich Gcp Pharmacology Pharmacovigilance Quality Assurance Clinical Research Clinical Data Management Anda Protocol Regulatory Affairs Pharmaceutical Industry U.s. Food And Drug Administration Standard Operating Procedure

Atul Bonde Education Details

Frequently Asked Questions about Atul Bonde

What company does Atul Bonde work for?

Atul Bonde works for Dr. Reddy's Laboratories

What is Atul Bonde's role at the current company?

Atul Bonde's current role is Lead DQA - Clinical and Pharmacovigilance at Dr. Reddy's Laboratories.

What is Atul Bonde's email address?

Atul Bonde's email address is at****@****pla.com

What schools did Atul Bonde attend?

Atul Bonde attended Annamalai University, Mgvm College Of Pharmacy, Nasik. Pune University.

What skills is Atul Bonde known for?

Atul Bonde has skills like Medical Writing, Cro, Sop, Clinical Trials, Clinical Study Design, Fda, Ich Gcp, Pharmacology, Pharmacovigilance, Quality Assurance, Clinical Research, Clinical Data Management.

Who are Atul Bonde's colleagues?

Atul Bonde's colleagues are Gowri Prasad, Raj Kumar Varma, Sanjeev Kumar, Pardeep Shetty, Shreyas Reddy, Basa Veera Venkata Satyanarayana Reddy, Yandapalli Krishnamohan.

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