Nature Scientist uses efficient state-of-the-art equipment to ensure the highest standards of product quality at the lowest possible production costs. Our products are carefully manufactured according to the cGMP guidelines

Our Lab testing capabilities include:

• Dust-contained, flexible facility designed for ease of change over, short processing times, and overall cost control
• Raw material, in process, and finished product testing
• Long term and accelerated stability testing
• Yeast and mold detection in raw materials and finished products
• Pathogen detection in raw materials and finished products
• Total plate count testing
• Yeast and mold detection in raw materials and finished product
• Quarantine, release, approvals and rejections
• Gas Chromatography (GC)
• High Pressure Liquid Chromatography (HPLC)
• UV Spectrophotometers (UV)
• Infrared Spectrophotometers (IR)
• Inductive Coupled Plasma Spectrophotometer (ICP-OES)
• ICH Stability Chambers
• Disintegrator
• Tablet hardness tester
• Incubators
• Autoclaves

Good Manufacturing Practices (GMP)

Quality Assurance

GMP refers to US Food and Drug Administration’s Good Manufacturing Practice Regulations. These are promulgated under the authority of the Federal Food, Drug and Cosmetic Act, and have the force of law.

These regulations require that manufacturers, processors, and packagers of drugs and medical devices take proactive steps to ensure that their products are safe, pure, and effective.

GMP regulations require a quality approach to manufacturing, enabling companies to minimize or eliminate instances of contamination, lack of uniformity, or poor quality.

As a result, consumers are protected from purchasing a product which is not effective or is dangerous. Failure to comply with GMP regulations can result in very serious consequences for non-compliant firms, including recall, seizure, fines, and jail time.

GMP regulations address issues including record keeping, personnel qualifications, sanitation, cleanliness, equipment verification, process validation, and complaint handling.

GMP calls for a process that starts with performance standards, includes training of key management and technical staff, auditing of performance, and reinforcement of findings on a repetitive basis.

GMP is also referred to as “cGMP”. The “c” stands for “current”, reminding manufacturers that they must employ technologies and systems which are up to date in order to comply with the regulation. Systems and equipment used to prevent contamination mix ups and errors which may have been “top of the line” 20 years ago may be less than adequate by today’s standards.