Lucid Solutions, Inc., founded in 1996, was established to take technical experience in chemistry and toxicology into the realm of quality assurance for the medical device and pharmaceutical industries.  We have provided compliance consultation on startups as well as consultation on specific tasks for large product development organizations.

Auditing remains our core service.  Our audits help our clients understand their level of compliance and also identifies areas prime for improvement, before the issue reaches a regulator or impacts the product pipeline.

We perform on-site audits of client facilities and operations and vendor facilities.  We also perform audits of study documents and technical reports from our office.  Email and FedEx provide all the communication needed to perform most document audits.  With both systems, Lucid maintains complete confidentiality and control over our client's information.

 Auditing is our main focus

 ● Clinical Audits

 ● Vendor Laboratories

 ● Laboratory Documentation

 ● Stability Test Results

 ● Batch Records

 ● Equipment Validations

 ● Manufacturing Facilities

 ● Common Technical Documents

 ● Case Report Forms

 ● Databases

 ● Statistical Outputs and Processing

 ● Pre-FDA Inspection Preparation Audits

 ● In-Process and Release Testing

 ● SOPs and Records

 ● TK/PK Reports

 ● Clinical Study Reports

  ©  2008 Lucid Solutions, Inc.  All Rights Reserved.