PharmXL International Pvt. Ltd.
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Personal Information
Unternehmen/Arbeitsplatz
Noida, Uttar Pradesh India
Branche
Medical / Health Care / Pharmaceuticals
Webseite
www.pharmxl.com
Info
We are an emerging life sciences consulting company, serving Globally. We provide support to our clients from pharmaceutical and Healthcare field, with our complete range of regulatory services for Drug and Medical Devices. We offer CRO services like Clinical research and trials; Regulatory support in obtaining registration, approval, import license etc; Pharmacovigilance services and Post-Marketing surveillance and medical writing services to our clients. PharmXL provides exceptional value to the clients by rendering variety of top-quality, cost-effective, customized, innovative, and timely healthcare services.
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safety adverse drug experience icsr adverse drug reaction drug safety pharmacovigilance fsca materiovigilance programme of india mvpi cdsco periodic safety update report psur regulations india individual case safety reports adverse event device safety matériovigilance medical device medical devices medicine anda nda pv rmp pader compliance reporting 21 cfr 314 adr cder fda pharma pharmaceutical
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Pharmacovigilance sytem in United States of America (USA)

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Personal Information
Unternehmen/Arbeitsplatz
Noida, Uttar Pradesh India
Branche
Medical / Health Care / Pharmaceuticals
Webseite
www.pharmxl.com
Info
We are an emerging life sciences consulting company, serving Globally. We provide support to our clients from pharmaceutical and Healthcare field, with our complete range of regulatory services for Drug and Medical Devices. We offer CRO services like Clinical research and trials; Regulatory support in obtaining registration, approval, import license etc; Pharmacovigilance services and Post-Marketing surveillance and medical writing services to our clients. PharmXL provides exceptional value to the clients by rendering variety of top-quality, cost-effective, customized, innovative, and timely healthcare services.
Tags
safety adverse drug experience icsr adverse drug reaction drug safety pharmacovigilance fsca materiovigilance programme of india mvpi cdsco periodic safety update report psur regulations india individual case safety reports adverse event device safety matériovigilance medical device medical devices medicine anda nda pv rmp pader compliance reporting 21 cfr 314 adr cder fda pharma pharmaceutical
Mehr anzeigen