Liquent and Take Solutions team on regulatory submissions

By Gareth Macdonald

- Last updated on GMT

Related tags Pharmacology

Liquent and Take Solutions team on regulatory submissions
Liquent and Take Solutions say their new partnership provides pharmaceutical firms with an efficient, cost effective outsourced solution for regulatory publication and submissions.

Liquent VP of sales and marketing Jeff Huntsman told Outsourcing-pharma that drug firms often lack in-house capacity to effectively manage the production of regulatory documents and that was a key driver for the deal with electronic submissions specialist Take Solutions.

He explained the alliance combines Liquent's regulatory expertise with Take's existing infrastructure to provide efficiencies adding that "Take is a very strong partner from a standpoint of having offshore resources and [of working within] compliance and efficiency guidelines.​"

Huntsman went on to say that Liquent is seeing considerable demand from regulatory services from large pharma firms, particularly for “non-strategic” products where the challenge is to produce the required regulatory documents in as efficient a way as possible.

He also said that, while this market is strong in Europe and the US, Asia has been slower to adapt to the eCTD model and as a result there has been less demand for outsourced submissions solutions.

Related news

Show more

Related products

show more

How a Clinical MDR Helps with Data Quality

How a Clinical MDR Helps with Data Quality

Formedix | 16-Jan-2023 | Technical / White Paper

This article covers the many ways a clinical metadata repository helps with data quality in the clinical trial process, and how it ultimately helps to...

Optimizing Adherence in DCTs

Optimizing Adherence in DCTs

PPD - Decentralized Clinical Trials | 12-Jan-2023 | Technical / White Paper

Prioritizing greater patient-centricity and creating an opportunity to reach unprecedented patient groups, decentralized and hybrid clinical trials are...

PPD is Supporting Complex EU DCTs

PPD is Supporting Complex EU DCTs

PPD - Decentralized Clinical Trials | 05-Jan-2023 | Technical / White Paper

PPD supports European DCTs and clinical trial sponsors with a holistic and comprehensive approach

What should a clinical metadata repository do?

What should a clinical metadata repository do?

Formedix | 14-Dec-2022 | Technical / White Paper

Choosing a clinical metadata repository (MDR) software can be a tough task as the capabilities and features of your chosen MDR could make or break your...

Related suppliers

Follow us

Products

View more

Webinars