Email: enquiries@bioventurescl.com

Regulatory Affairs & Product Development Services

The Application of Strong Scientific Understanding

Regulatory publishing: eCTD, NeeS or Paper Output

BioVentures Consulting Limited offers regulatory publishing services (eCTD, NeeS or Paper Output) through Mark Willoughby who leads the Regulatory Operations team. The team has over 10 years’ combined experience in the field of Regulatory Operations, and is fully equipped and able to produce high quality, compliant submissions whatever the situation.

BioVentures Consulting Limited has the capability for remote publishing facilities applicable for eCTD, NeeS or Paper Output. If high quality, fully compliant submission output is all you require then our UK-based remote publishing service may be for you.

We have created submissions for some of the highest profile products for several of the world’s largest pharmaceutical companies

Using our own hardware and licensed software, we are able to process your submission documents into eCTD, NeeS, paper or nonstandard output and transfer it back to you using our secure FTP site.

Our eCTD output is guaranteed to be compatible with any eCTD build tools and agency viewers. Our remote publishing service is available on a pay-per-submission basis, or for a set duration, guaranteeing total flexibility of service.

We have created submissions for some of the highest profile products for several of the world’s largest pharmaceutical companies, so you can rest assured that your work will be left in capable hands.

Whether you manage a large Regulatory Affairs department in a large pharmaceutical company or are looking to outsource all of your Regulatory Operations work BioVentures Consulting Limited is able to deliver a range of services to suit a variety of needs.

For more information contact us on: This email address is being protected from spambots. You need JavaScript enabled to view it.

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