Generic Pharmaceuticals Regulatory Function Diligence (please apply for immediate consideration)

Project status
Project start date
12 Mar 2018
Project posted
26 Feb 2018 17:51
Project duration (approx.)
5.0 Days
Budget (approx.)
£8000 (fixed cost)
Level of Experience
Senior
Industry
Pharmaceuticals
Area of expertise
Corporate Finance / M&A
Consultant location
On-site
Location
United Kingdom
Languages
English (Essential)

Objectives and Key Deliverables

We are a global management consulting firm and engaged by a private equity client evaluating a potential acquisition of a generic pharmaceuticals business.

As part of the due diligence process the client has asked us to review the regulatory operations of the target business.

The target business’ business plan includes:

- Re-transfer of production currently undertaken by CMOs/ the parent company into the production facilities of the target
- An increase in output and productivity in bringing new products to market/ delivering market authorisations

Consultant requirements:

We are looking to engage with a professional with experience in the regulatory function of a major generics business and with experience dealing with regulators in particular the EMA (and the FDA). Ideally the professional would also have experience in M&A processes and evaluating the regulatory functions of target businesses.


Project deliverables:

The consultant will attend a site visit in Prague next week (Wednesday March 14), participate in a regulatory session and then produce a red flags report. The expected workload will be around 5 days. Therefore, we are looking for a consultant immediately.

Logistics:

The consultant will fly to Prague for the site visit (fly in Tuesday evening and fly out Wednesday evening). The rest of the work can be done remotely or in our London office. Travel & Expenses are covered.

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