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Service Providers & Outsourcing

Global Experts in Pharmacovigilance

More than 18 years of experience providing Pharmacovigilance and Pharmacoepidemiology services, our of global experts include highly qualified, trained and experienced professionals from the corporate and academic world.

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Experience

More than 18 years of experience providing Pharmacovigilance and Pharmacoepidemiology services, our of global experts include highly qualified, trained and experienced professionals from the corporate and academic world.

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Quality

By understanding and improving operational processes; identifying customer requirements quickly and systematically; establishing valid and reliable service performance measures and measuring customer satisfaction.

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Innovation

Research and innovation is an important part of Symogen business development process. We focus in several research projects to continually improve and enhance the quality of our services and to meet the high requirements of our customers.

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About Us

Partner with us for quality Pharmacovigilance solutions

With an impeccable track record of quality and highly ethical practices, Symogen serves global clients that include start-ups, mid-sized enterprises and fortune 100 companies, from its delivery centres in Europe and United States.

  • Pharmacovigilance
  • Pharmacoepidemiology
  • Complete Case Management
  • PV/Drug Safety Services
  • Product's Safety Database
  • Medical Writting
  • Quality Assurance
  • Signal Detection
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Services

The best in class pharmaceuticals, medical devices and biotech safety services

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Pharmacovigilance Services

Currently providing comprehensive pharmacovigilance support to clients (MAH’s) while covering various therapeutic areas, which includes oncology, psychiatry, fertility, infectious diseases, endocrine diseases, cardio vascular diseases etc. Symogen has endeared itself to customers by constantly pursuing perfection in the pharmaceutical, biotech and medical devices space.

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Medical Device Vigilance & EU MDR

Our team of Medical Device vigilance experts are well versed in the differing requirements for CE-marked and non-CE marked devices, Implantable Medical Devices, In Vitro Diagnostic Medical Devices and drug-device combination products following both European Union (EU) and FDA Guidelines.

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Safety Database Solutions

Symogen offers Safety Database Solutions fully dedicated to the management of Adverse Events related to pharmaceutical products, Medical Devices & Cosmetics

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Quality Assurance Services

We have expertise in covering whole range of compliance solutions including PV audit planning, reporting, ADR reporting metrics, CAPA (Corrective and Preventive Action) development, GVP and GCP system inspections, audit and reporting.

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Pharmacoepidemiology Services

With years of experience, our expert team of epidemiologists are no strangers to real-world data. If you’re looking for advisory services; registry study; a literature review; prospective observational research; you can trust our high-quality driven experts to provide, scientifically-meticulous epidemiology support.

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Medical Writing

Team of specialist medical writers with an in-depth knowledge, skills and experience of pharmacovigilance writing. Adhering to scientific writing standards, they compile, write, edit and produce a wide range of medical documents, including aggregate reports, risk management plans, signal evaluation reports, labelling documents, ICSR narratives, clinical overview & clinical summary, pharmacovigilance plans and more.

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Benefits-Risk Management Service

Symogen provide support and expertise to clients in setting up and performing different types of Benefit-Risk Analyses

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Regulatory Strategy Help Services

Regardless of where your product is during its life cycle, with Symogen’s in-depth experience and expertise, we provide quick, effective and strategic regulatory solutions for our clients.

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Get in Touch

Leverage high-end PV system deployment globally with fully-equipped safety database solutions implemented with innovative technologies by a team of experienced & trained professionals!

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We Are Here For You

Full-Scale solutions for your Pharmacovigilance requirements throughout clinical trials phases, as well as post-marketing processes covering high-quality data collection, assessment and reporting.

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Years in Business

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Aggregate Reports

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Symogen Means

Experience,Quality,Innovation

Comprehensive Pharmacovigilance services from “development to market”, incorporating innovative technologies, quality procedures and experienced input ensuring maximum success with cost-effectiveness.

Meet Our Team

Led by a Team of Passionate Experts

Our team consists of industry experts having in-depth niche experience, expertise in clinical data and global capabilities. Through our global offices, the team’s mission is to help the clients with full range of pharmacovigilance consulting and clinical development support.

Meet All
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Dr. Arun Biswas

Managing Director and Chief Medical Officer
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Dr. Pipasha Biswas

Executive Director & QPPV
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Bobby Mahajan

Head of Global PV Operations
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Pedro Berrio

IT Director
Testimonial

What’s Clients Response About

News Update

Symogen News & Blog

Get the latest in industry insights, regulatory updates, clinical norms, research and studies and business information.

December 26,2019
By: admin

AI in Pharmacovigilance

Key Takeaways:

  1. Adverse Event reporting has increased substantially in the last few years.
  2. Clients and CRO’s are both looking to reduce costs and increase efficiencies.
  3. ...

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November 29,2019
By: admin

Medical Devices

Key Takeaways:

  • Intense scrutiny of medical devices by regulatory authorities (EU-MDR and FDA) increasing both in Europe and US.
  • High quality data driven clinical research, ISO...

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September 26,2019
By: admin

Pharmacovigilance Outsourcing

  • The pharmacovigilance industry is poised for a quantum growth in 2020
  • Complexities are increasing due to new drug launches and higher degree of regulatory requirements.
  • ...

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We'll ensure you always get the best Results

Working with a tailored approach specific to your business requirements, we collaborate with clinical research, development, regulatory affairs, risk management plans giving you optimal PV system end-results.

Get in touch with us to access advanced technologies, high-end & in-depth resources, effective governance and profound assessment, monitoring and reporting solutions.

+44 (0) 1628 566511

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