Project Management
With nearly two decades of experience in corporate project management, LSP is
well-qualified to assist in defining and assembling the elements needed for an
effective project team and execution strategy, and to help with follow-through
and periodic assessments of progress. |
Manufacturing and Quality
The success of LSP’s principals in establishing quality systems and in
overseeing product development leading to cGMP drug production, well qualifies
us to assist with your quality and production needs.
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Qualify and select contract testing laboratories
and production facilities
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Assist with facility design and process
development
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Develop test methods and final product
specifications
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Design stability testing programs; select test
parameters
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Structure corporate quality system
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Assess compliance with current Good
Manufacturing Practices (cGMP; for drugs) and Quality System Regulation
(device)
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Provide on-site instruction in cGMP- and ICH-compliant
systems and practices
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Assist with inspections by FDA, the Nuclear
Regulatory Commission (NRC) or foreign regulatory agencies
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Review or prepare validation protocols and
reports
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Review or prepare standard operating procedures
(SOPs)
Other Services
With thirty years of experience formulating searches of technical and biomedical
databases, LSP can provide efficient and effective literature and patent
searches, and can also prepare review papers based on the search results.
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