Good Day Plus

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Quality Policy

We are fully committed to creating only high-quality, safe and effective nutritional supplements. Dedicated to first value your health, before our own profits.

Our Core Quality Policy Of Dietary Supplement Products

Good Day Plus’s healthcare dietary supplements products are manufactured by the Regulation of New Zealand Minister of Health and GMP-certified standards.

 

Good Manufacturing Practice (GMP) is a total manufacturing and quality assurance system that sets the standards for operation of the entire company. GMP is internationally accepted for the production of quality products.

 

Good Day Plus’s products have a wider market opportunity, higher levels of safety assurance and will:

 

  • be fit for their intended use
  • not place the user at risk
  • confirm to all the statutory legislation and guidelines
  • comply with the requirements of the marketing authorization

 

We follow strict guidelines with regard to cleanliness, production procedures and a host of other quality parameters to ensure that the product arrives in the hands of the consumer in perfect condition. Operating to this standard will allow us to export our products overseas and customers can trust our brand.

Licenses & Certificates

Good Day Plus’s healthcare dietary supplements products are manufactured by Regulation of New Zealand Minister of Health and GMP certified standards.

Quality Policy

Australia and New Zealand are well known internationally for having amongst the strictest and most comprehensive regulatory controls in the world to ensure that therapeutic and food products conform to the highest standard of quality, efficacy and safety. Our strict Quality Management Systems are formalised, practical and provide a high level of traceability. To ensure that our systems are effective, we conduct regular internal audits and are subjected to regular audits by government authorities. These audits form part of our continuous improvement process.

This quality system encompasses the entire manufacturing process from ordering and receipt of raw materials to packaging and dispatching, including the entire manufacturing process. Each step is controlled by Standard Operating Procedures to guarantee full traceability of materials, consistency in manufacturing of goods and reliability in all outcomes. The systems have been designed to meet and exceed the expectations of our valued customers.

Our respected customers have come to rely on our commitment to the delivery of on-time high quality products. GMP Pharmaceuticals is dedicated to providing advice as well as products related to vitamin, herbal, fish oil, dry dairy & many other complimentary medicine & dry dairy fields.

Laborarory Policy

Our in-house laboratories include current state of the art instruments such as:

• Thin-layer Chromatography (TLC)
• High Performance Thin-layer Chromatography (HPTLC)
• UV-Visible Spectrophotometry (UV-Vis)
• Mass Spectrophotometry (MS)
• Infra-red Spectrophotometry (FTIR)
• Ultra High Performance Liquid Chromatography (UHPLC)
• High Performance Liquid Chromatography (HPLC)
• Gas Chromatography (GC)
• Automated Dissolution Apparatus

 

These are in conjunction with the well known traditional analytical techniques such as titrations, gravimetric analysis & other wet chemistry assays. GMP Pharmaceuticals also has commercial & technical arrangements with a number of Australia’s & New Zealand’s leading laboratories to provide highly specialised analyses. This array of instruments & technical abilities are intended to ensure that the products that we manufacture on behalf of our customers provide the intended therapeutic benefits.