- Adverse Event reporting has increased substantially in the last few years.
- Clients and CRO’s are both looking to reduce costs and increase efficiencies. ... Learn More
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.Learn More
By understanding and improving operational processes; identifying customer requirements quickly and systematically; establishing valid and reliable service performance measures and measuring customer satisfaction.Learn More
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.Learn More
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.
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.Learn More
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.Learn More
Symogen offers Safety Database Solutions fully dedicated to the management of Adverse Events related to pharmaceutical products, Medical Devices & CosmeticsLearn More
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.Learn More
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.Learn More
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.Learn More
Symogen provide support and expertise to clients in setting up and performing different types of Benefit-Risk AnalysesLearn More
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.Learn More
Leverage high-end PV system deployment globally with fully-equipped safety database solutions implemented with innovative technologies by a team of experienced & trained professionals!
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.
Years in Business
Comprehensive Pharmacovigilance services from “development to market”, incorporating innovative technologies, quality procedures and experienced input ensuring maximum success with cost-effectiveness.
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
Professionals with an abundance of pharmacovigilance experience used to produce quality work in a timely fashion. Symogen values success of the team and is genereous in sharing their experience, knowledge and time.
Excellent knowledge in pharmacovigilance especially in Signal Detection and Risk Management. Approachable and executes work meticulously, accurately and on time.
Well-known for high-quality and compliant work among Japanese pharma companies. Managed large projects in various countries. Highly-experienced, energetic, straightforward, dedicated, honest, and down-to-earth professional team who can turnaround difficult situations in pharmacovigilance with ease.
Opportunity to face one of the Pharmacovigilance audit in India conducted by Symogen. It was very good experience for me and the experience shared provided a lot of in-depth understanding of Pharmacovigilance practices. A great person and team to work with and one can grasp a lot of technical information from Dr. Pippa
Excellent and deep knowledge on all aspects of Pharmacovigilance & Risk Management including safety evaluation, signal detection and regulations. Delivers high quality work on every project; extremely punctual, inventive, consistent and reliable. A great asset, great understanding in this field and implements projects to the highest quality.
Deep understanding of safety risk management; is a real asset to companies needing pharmacovigilance support.
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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.Contact Us