Pharmacoepidemiology1

Pharmacoepidemiology

Pharmacoepidemiology is the investigation of the use and impacts of medications in vast quantities of individuals; it gives an appraisal of the likelihood of helpful

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pharmco

Pharmacovigilance Compliance

According to the definition of the World Health Organization (WHO), Pharmacovigilance (PV) is “the science and

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Document writing and Data Analysis.

Document writing and Data Analysis

Information investigation is the procedure of creating answers to questions through the examination and translation of information.

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Pharmacoepidemiology2

Data Management Solutions

Over the span of your trial, the clinical checking bunch has the backing of our committed medicinal observing group of experienced experts crosswise over helpful

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marketing

Post Marketing Pharmacovigilance

Pharmacovigilance (PV) is “the science and activities relating to area, examination, perception and evasion of adversarial effects

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Medical Information

At Vigilare biopharma we provide a flexible, responsive and personnel experience to the clients .We have client across the globe. Our team is well trained and knowledgeable

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liaison support1

Medical science liaison support and representation

Scientific Experts are people who are noted for their ability in a specific range and therefore,have special needs for

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Medical writing

Medical writing

Medical Writing is an indispensable part of clinical exploration. Our Medical Writers work closely with our associates in the biostatistical, pharmacovigilance

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SALES TRAINIG

Sales Training

Pharmaceutical sales delegates spend pharma-sales-training most of their time outside, talking with pharmacists and hospital personnel doctors to promote

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clinical-trails

Clinical Trails

Clinical Trails leverages our unique partnering philosophy and team structure to deliver effective, end-to-end collaboration, training, and resource planning

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Preclinical safety assessment

Our Team of consultants helps our clients develop clinical testing plans consistent with the stage of preclinical development and FDA requirements.

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Clinical Safety Surveillance

Clinical Safety Surveillance

Assessment and reporting of all the safety events to the global regulatory authorities, including EudraVigilance reporting and EU e-reporting

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Riskmanagement

Risk Management

The significant costs of research and development, the risks involved in manufacturing and testing, and quickly changing environmental laws

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product complaints

Product Complaints

Maintaining an adequate complaint handling system is more than just a requirement, it is a good quality practice that can help assure your product continues to meet

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Registry Activities

VIGILARE BIOPHARMA’s experience handling and managing pregnancy registry activities is unsurpassed. We support handling complete registry case reporting aligned activities

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