Seerpharma.com.au :: Pharmaceutical Consulting & Training :: Validation, GMP & Compliance UK | Singapore

   

SeerPharma announces a new service: Managed professional resources for the life sciences industry

SeerPharma is the leading and trusted life sciences professional consultancy service in Australia and Asia. Our team of expert consultants deliver top level compliance advice and practical solutions, supported by strong industry training and knowledge transfer. Our approach to client support has always been to transfer knowledge, add value and strengthen procedures and processes, so that the client is in control.

We have expanded our services to include client access to Professional Resources for short-term projects, implementation support, specific roles or temporary technical needs. We contract our professional services team, or individuals, to implement and deliver agreed solutions.

  • Our employees are qualified into the position. They are GMP and project ready.
  • A senior SeerPharma consultant initially works with the client to define the contract/project terms and the role, scope and budget parameters.
  • We conduct regular review meetings with the client project leader to ensure that our representative stays on track, adds real value and is delivering to the project plan.
  • We offer access to the SeerPharma library of compliance solutions, where needed, to save time and money.
  • Near completion of the contract/project, we provide a plan to ensure knowledge and skills transfer from SeerPharma to the client.

Why turn to SeerPharma for your resource solutions?

  • We have a trusted and proven reputation for delivery and practical solutions.
  • We have short-term or long-term cost competitive professional resources available.
  • We have a consistent track record for strong customer focus and value added solutions.
  • We understand that reputation is everything and delivery on expectations is essential.


Call us if you have a need for well-managed professional resources for validation projects, technical/SOP writing, compliance upgrades, QA/QMS/Regulatory Affairs associates, IT compliance and GMP-related support staff on a project or temporary basis.

 

   
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