MRA Closed for Presidents Day

Microbiology Research Associates offices will be closed for the Presidents Day holiday, Feb. 19. We will reopen for normal business hours Feb. 20.

Do You Have Your Testing Program in Place?

With the continuous evolution of regulations in the compounding industry, properly validated testing methods are essential to maintain your product claims.

At Microbiology Research Associates, we’ll put our USP <797>, USP <800> and cGMP expertise to work for you. We offer full service compliance capabilities for pharmacists at 503A and 503B facilities to ensure a state of environmental control. And MRA staff are experienced in performing USP <71> and USP <85> tests.

Contact MRA to learn how our USP and cGMP expertise can help you.

Cleanroom Classification Influences Layout

A cleanroom’s classification defines the level of cleanliness that must be met and maintained. And while it does not determine the cleanroom layout, it does influence it.

A January 2018 article from Controlled Environments Magazine details many design options and requirements for various sizes and ISO levels of cleanrooms.

Microbiology Research Associates can validate your new or upgraded cleanrooms, and can verify the design, operational and performance specifications. Once your cleanroom is validated, MRA also can set up a cleaning and disinfectant program to maintain proper cleanliness.

Contact MRA to learn how we can help you with your cleanroom validation.