We offer superior science-backed quality, potency, and effectiveness.

Science-Backed Quality and Effectiveness

  • Bioclinic Naturals professional health supplements offer Health Care Practitioners superior science-backed quality, potency, and effectiveness.

  • Organic farming, in-house research and development, and strict adherence to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) are all components of the total quality control used to produce Bioclinic Naturals products.

  • Natural Sources

    We use raw materials that are sourced from the world’s most trusted suppliers. Audits are done before a supplier is contracted and all raw materials are extensively tested before they are accepted for use in Bioclinic Naturals products. 

  • Above and Beyond GMP Requirements

    Bioclinic Naturals facilities meet Good Manufacturing Practices (GMPs) guidelines, as well as the strict regulations of the Australian Therapeutic Goods Administration (TGA). Bioclinic Naturals complies with all aspects of these GMP regulations, ensuring that only the highest quality finished goods reach our customers and their clients.

  • What GMP means to the Health Care Practitioner

    The guidelines for manufacturing mean that Bioclinic Naturals offers quality assurance, analysis and testing, proven procedures, documentation and validation, appropriate and approved equipment and facilities, as well as all required employee training and participation in meeting quality control standards. What this means for a Health Care Practitioner is that every Bioclinic Naturals product provides known, consistent, health benefits based on researched and measurable levels of known therapeutic nutrients and botanicals.

  • Laboratory “Gold Standards”

    Bioclinic Naturals laboratories also meet Good Laboratory Practices (GLP) guidelines that require strict adherence to specific quality standards. These GMP and GLP guidelines, as well as our attention to quality assurance, ensure that Bioclinic Naturals products are pure, potent and contain exactly what is on the label – no more, no less. GLP means that we meet the following commitments:

Our Gold Standards Commitments

Good Laboratory Practices (GLP) means that we meet the following commitments:

Stability Program

Stability Program

Products are tested throughout the shelf-life and for one additional year to guarantee that the potency always matches the label claim.

Analyst Training Program

Analyst Training Program

The Analyst Training Program provides practitioners with evidence-based product education and clinical training to support better patient care.

Standard Operating Procedures

Standard Operating Procedures

A set of written procedures for conducting every operation in the laboratory.

Method Validation

Method Validation

All methods are validated to ensure consistency of analytical parameters including selectivity, linearity, range, accuracy and recovery, precision and ruggedness.

Raw Materials Testing

Production and Post-Production Testing

Production and Post-Production Testing

The manufacturing department must meet or exceed its own set of quality control requirements. Finished products are tested for weight variation and hardness throughout the production run. These tests ensure that every run, and every batch, is consistent from beginning to end.

Finished Product Testing

Potency Testing

The same methods are used as in raw material testing, only the product may require multiple potency tests for each vitamin, depending on the formulation. In the case of a multivitamin, up to 12 potency tests may be conducted.

Microbial Testing

Micro testing is performed using USP methods. It is intended to protect consumers from deadly pathogens and demonstrate raw materials and finished products are in a sanitary manner. Common testing includes aerobic plate count, yeast, and mold, E. coli, Salmonella, and S. aureus.

Content Uniformity

This test involves determining the potency of 10 individual tablets or capsules to determine the uniformity of dosage units. The Relative Standard Deviation of the potency results may not exceed the USP limit of 6%.

Disintegration

Using a USP-compliant disintegration apparatus, meant to simulate the movement of the human stomach, we determine the time for a representative sample to disintegrate. In general, for tablets and capsules they must disintegrate within 30 minutes in water medium. For more complex formulas disintegration within 45 minutes within a water or simulated gastric medium is acceptable. Extended release tablets/capsules are tested to withstand the simulated gastric medium and disintegrate in simulated intestinal fluid. This is a summary and for exact requirements USP method should be referred to.

Weight Variation

Using a representative sample of the finished product (20 tablets or capsules), the weights are recorded and the average is obtained. The weight variation from the average may not exceed 5% for tablets and 10% for capsules.

Identification

These tests are performed using the same methods as used for the raw materials.