Quality control is priority number one at Your Solution Compounding Pharmacy, starting with a state of the art Sterile Facility, which is pressure, temperature and humidity controlled, as well as equipped with Class 100 laminar flow hoods. We also adhere to the latest PSA and USP<797> standards. All of our raw materials are of a pharmaceutical grade which have gone through stringent batch testing, and are therefore certified to be of the highest and correct purity and strength required for compounding.
Our sterile, prescription quality control procedures are as follows:
Ingredients are shipped to our facility with Certificates of Analysis verifying product integrity.
Ingredients are stored in a carefully controlled environment prior to usage.
Our self developed and unique Patient Ordering System (YSO) software takes quality control to a new level.
At the time of compound preparation, the ingredients, lot numbers and expiration dates are recorded.
All staff involved in the sterile compounding process are trained and accredited in the preparation of aseptic compounds and are annually re-certified for proficiency.
Prescriptions are checked three times by pharmacists during the compounding process, with the last step after preparation, for color and/or clarity, consistency, packaging integrity, and readability of label instructions, thus enabling patients to easily measure required doses accurately.