PVpharm

www.pvpharm.com

www.pvpharm.com https://www.pvpharm.com/careers -PVpharm provides consultancy services in Pharmacovigilance for the Pharmaceutical Industry -We work independently or in collaboration with other PV service providers / CRO's -EU QPPV service -Local QPPV services for Spain -Training pharmacovigilance and GVP -Pharmacovigilance GVP Audits -EudraVigilance EVWeb and the XEVMPD (eXtended EudraVigilance Medicinal Product Dictionary). Possibility internal certified on-site training for pharmaceutical companies. -Registration with Eudravigilance for Pharmaceutical companies. -Introduction of information of medicinal products in the XEVMPD. -Development of IDMP implementation consultancy services. -Case management of suspected adverse reactions, including contact with reporters, MedDRA coding, Data Entry and Electronic reporting to health authorities. -Literature searches for Pharmacovigilance. -Implementation of the company's Pharmacovigilance system, including Standard Operating Procedures for Pharmacovigilance (SOPs / PNTs). -Development and revision of Pharmacovigilance documents, including Periodic Safety Update Reports (PSURs), Risk management plans (RMPs) and Elaboration of the Pharmacovigilance System Master File. JOBS: please visit our website at www.pvpharm.com

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www.pvpharm.com https://www.pvpharm.com/careers -PVpharm provides consultancy services in Pharmacovigilance for the Pharmaceutical Industry -We work independently or in collaboration with other PV service providers / CRO's -EU QPPV service -Local QPPV services for Spain -Training pharmacovigilance and GVP -Pharmacovigilance GVP Audits -EudraVigilance EVWeb and the XEVMPD (eXtended EudraVigilance Medicinal Product Dictionary). Possibility internal certified on-site training for pharmaceutical companies. -Registration with Eudravigilance for Pharmaceutical companies. -Introduction of information of medicinal products in the XEVMPD. -Development of IDMP implementation consultancy services. -Case management of suspected adverse reactions, including contact with reporters, MedDRA coding, Data Entry and Electronic reporting to health authorities. -Literature searches for Pharmacovigilance. -Implementation of the company's Pharmacovigilance system, including Standard Operating Procedures for Pharmacovigilance (SOPs / PNTs). -Development and revision of Pharmacovigilance documents, including Periodic Safety Update Reports (PSURs), Risk management plans (RMPs) and Elaboration of the Pharmacovigilance System Master File. JOBS: please visit our website at www.pvpharm.com

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Country

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City (Headquarters)

Almería

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Employees

11-50

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Founded

2014

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Social

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Potential Decision Makers

  • Founder and Chief Executive Officer at Pvpharm , Eu Qppv , Pharmacovigilance Consultant

    Email ****** @****.com
    Phone (***) ****-****
  • Deputy Qppv / Lcppv , Pharmacovigilance Officer

    Email ****** @****.com
    Phone (***) ****-****
  • Pharmacovigilance Senior Officer

    Email ****** @****.com
    Phone (***) ****-****
  • Human Resources and Finance Specialist

    Email ****** @****.com
    Phone (***) ****-****

Technologies

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