Quality
Our state-of-the-art 503A pharmacy, we are held to the standards of USP 797. Exceeding these standards is our commitment to our trusted practitioners and patients.
Standard of our quality department
A 5,500 square foot cleanroom with certified ISO-8, ISO-7 and ISO-5 compounding rooms
USP 800 ready facility with negative pressure rooms for hazardous drug handling, storage and compounding.
PCAB Accreditation in sterile and non-sterile compounding
Analytical laboratory testing for sterility, endotoxin, potency and stability studies
Formulation Experts
FDA registered chemicals suppliers
Pharmaceutical automation
Equipment IQ/OQ/PQ validations
Compounding experienced pharmacists and registered pharmacy technicians
Pharma Manufacturing experienced personnel
Robust Environmental & Personnel Monitoring program
Staff Microbiologists
Cleanroom Engineering Experts
30+ point production process; from formula development to batch release
Routine USP standard aseptic personnel trainings and assessments
ACPE personnel trainings
Bi-annual and annual cleanroom equipment calibrations and certifications
Facility Preventative Maintenance Program
Why Compounding
As an industry leader in compounding, Hallandale Pharmacy's growth has been propelled by the increase in demands for custom medications. These medications are either no longer available on the commercial market and/or further customized to the specific medical needs of patients. There is no one size fits all when it comes to medication. Modern medicine has evolved to recognize the need for custom medication formulations allowing greater patient specific medical care provided by compounding pharmacies. Additionally, medication shortages have risen tremendously, a true impact on patient care. Compounding allowsfor filling the gaps that commercial medications cant fulfill.
