With more than 150 Life Science customers and 15 years as an Independent Software Vendor, Ennov strives at serving the pharmaceutical, veterinary and medical device industries.
We manage life science regulatory content
Our suite of applications covers a wide range of regulatory requirements
- Quality Management (EQMS)
- Regulatory affairs (eCTD submissions, RIM)
- Pharmacovigilance (human and veterinary)
- Clinical trials (EDMS, EDC, CTMS, eTMF)
- 21 CFR part 11 traceability and electronic signature
We work closely with regulatory authorities. Our regulatory intelligence and oversight enable us to keep our solutions always up to date with the latest regulatory requirements.
Consultants who understand your business
Our professional services team has extensive experience and expertise in the life science industry and will help you configure your solution to best suit your requirements.
More than 98% of our projects are delivered on time and within the initial budget.
To ensure the success of your projects, Ennov offers comprehensive training. We also offer to follow you during the submission of your first dossier.
We have teams to serve you in San Francisco, CA, Durham, NC, Cambridge, UK and Paris, FR.
Configurable solutions for a low risk and total cost of ownership
Our solutions are designed to allow configuration by domain experts, with no IT skills required. This helps control the risk and cost of implementing projects while ensuring the scalability of implemented solutions.
This approach helps our customers deploy our solutions for a very competitive TCO.
Flexible and modern technological platform
We provide cutting edge web technology for our users:
- Web interfaces for universal access
- Scalable, fast and responsive
- Mature, robust technology with hundreds of thousand of satisfied users worldwide