Complementary Prescriptions™ — Clinically Researched, Laboratory Tested, Maximum Purity

Quality Control
Complementary Prescriptions™ formulas are manufactured in a certified Good Manufacturing Practices (GMP) facility following the highest standards to ensure the quality from the purchasing of raw materials to the finished product. Complementary Prescriptions™ products adhere to all FDA, GMP guidelines for authenticity, potency, finished goods and documentation protocol. Our facilities are audited by independent outside agencies to certify and prove our compliance with GMP guidelines and quality assurance practices.
- GMP Standard Operating Procedures
Complementary Prescriptions™ follows all standard operating procedures (SOP's) inside the GMP manufacturing guidelines.
- Independent Certification of Analysis
All ingredients are quarantined upon receipt, pending independent certification of analysis. Both High Performance Liquid Chromatography (HPLC) and FT-NIR testing methods are used.
- Ingredient Tracking System
All ingredients received are quarantined and sampled for lab analysis. Once ingredients pass inspection, ingredients are coded and assigned tracking numbers. Production batch records are QC'd by quality control managers prior to the blending process, customized manufacturing software programs provide ingredient identification records.
- Manufacturing Enviroment
Our state of the art manufacturing production facility operates in sealed humidity- and dust-controlled individual rooms adhering to GMP standards.
- Equipment Sanitization Process
All Encapsulation and manufacturing equipment are dismantled and sanitized prior to every new capsule run to avoid cross ingredient contamination and ensure product safety.
- Capsule Validation
Each capsule is checked for accurate fill weight, structure integrity, color and polishing before bottling.