Quality Control
Quality Control Consulting by Microrite covers all measures taken, including the setting of specifications, sampling, testing and analytical clearance, to ensure that the raw materials, intermediates, packaging materials and finished pharmaceutical products conform with established specifications for identity, strength, purity and other characteristics.
- Management of Quality Control Function
- Designing efficient workflow systems for QC laboratories and testing
- Sampling plans and analysis
- Laboratory and stability protocols, data analysis and reports
- Developing and modifying test methods, SOPs, and specifications
- Establishing and revising raw material, in-process and product specification
- Setting up QC laboratory facilties
- Training
ON-SITE TRAINING
- Strategy for Investigating Microbial Contaminations
- Cleanroom Microbiology
- Contamination Control
- Environmental Monitoring, Tracking and Trending EM data and compiling meaningful EM Summary Reports
- Disinfectant Qualification and Cleaning Procedures
- Fungal Identification
1:30pm - 3:30pm Eastern Standard Time
1:30pm - 3:30pm Eastern Standard Time
1:30pm - 3:30pm Eastern Standard Time
September 19th and 20th, 2013
1:30pm - 3:30pm Eastern Standard Time
August 7th and 8th, 2013
Call Microrite: (408) 445-0507
Three Cs for Microrite
C1: Creativity - We believe that creativity, not additional capital, generates the most effective solutions. This is the reason why we use a risk based approach and quality by design approach in all our work.
C2: Communication - We have no secrets and give no surprises. We always will tell you what is happening and teach you everything we know. We communicate!
C3: Cost conscious - We help you succeed by treating your project as our business. Establishing phase specific systems to avoid overkill and overspending is our specialty.
Do it Once...Do it Right!
