Going to the 2016 International Society of Pharmaceutical Engineering (ISPE) Annual Meeting September 18-21, in Atlanta GA?
If YES, please plan to stop by Booth 818 to meet members of the Performance Validation team to learn about our expertise and how we might be able to help you on your current or future projects.… more
INDIANAPOLIS, June 14, 2016 /PRNewswire/ — Performance Validation is quickly making a name for itself in the environmental mapping industry. Storage chambers, warehouses, manufacturing facilities and laboratories are just a few environments where precise temperature and humidity control is an essential component of the operation, particularly in regulated life science fields.… more
For Immediate Release (Indianapolis, Indiana; March 4, 2016). Performance Validation is pleased to announce that Ms. Ashley Saberniak has successfully completed certification as a Certified Quality Improvement Associate.
The Certified Quality Improvement Associate is a professional who understands quality tools and their uses and participates in quality improvement projects. … more
Bruce E. Beck, Appointed as Board Advisor to Performance Validation’s Board of Managers
Performance Validation LLC (2015), I am pleased to announce the appointment of Bruce E. Beck to the position of Board Advisor to Performance Validation’s Board of Managers. Mr.… more
Indianapolis, IN (August 2015) Performance Validation, a nationwide leader in providing validation, commissioning, and quality services, today announced the promotion of Stephanie Welte to Principal Validation Engineer.
The Principal Validation Engineer advises clients on best industry practices; defines, plans and executes project work including research, evaluation, and/or solution development to achieve customer objectives; and lead project related functions defined by the customer in a manner that is consistent with Performance Validation’s values.… more
I am very happy to announce that I have been promoted to PhD Candidate! At Indiana Wesleyan University to be promoted to a PhD Candidate means that I have satisfactorily completed all course work and the comprehensive oral examinations. Written the proposal, which consists of the first three chapters of my dissertation, and satisfactorily completed the dissertation proposal seminar.… more
Milwaukee, Wis., 06/06/2015 — The Certification Board of ASQ is pleased to announce that Matthew Hopson has completed the requirements to be named an ASQ-Certified Six Sigma Green Belt, or ASQ SSGB.
As such, Matthew Hopson has reached a significant level of professional recognition, indicating a proficiency in and a comprehension of Six Sigma principles and practices.… more
PRESS RELEASE….August 22, 2014
The Indiana Medical Device Manufacturing Council (IMDMC) announced today that State Representative Kathy Heuer, (R) Columbia City, has been hired as their Executive Director.
IMDMC serves to represent the interests of its member medical device companies in the delivery of innovative, life-changing technologies to patients.… more
The presentations from ASTM International’s E55 Manufacture of Pharmaceutical Products Raw Materials in Biopharmaceuticals Workshop which took play May 21, 2014 in Boston, Massachusetts at Vertex Pharmaceuticals are posted to the E55 Committee Documents page (available to non-members here).
The Single Use Systems (SuS) Raw Materials Workshop was attended by over 60 international representatives with presenters from major biopharmaceutical companies, users, material suppliers and regulators to discuss the use of standards to support raw materials; the supply chain, change control management and systems qualification; extractable testing (SUT); single use technology and standards.… more
For Immediate Release (Indianapolis, Indiana; June 16, 2014). Performance Validation is pleased to announce that Ms. Stephanie Welte has successfully completed certification as a Certified Quality Auditor.
The Certified Quality Auditor is a professional who understands the standards and principles of auditing and the auditing techniques of examining, questioning, evaluating and reporting to determine a quality system’s adequacy and deficiencies.… more