Dietary Supplements Manufacturing Management
You don’t have time for mistakes, and you have to move quickly. Patients are depending on you.
Watch the case study
MasterControl Offers
4 Key Advantages for Life Sciences
Paperless Manufacturing
Paper is slowing you down. Our paperless manufacturing software automates batch records, device history records, recipes, and more to help you work more efficiently and get your products to market faster.
Mobile Access
MasterControl allows users to access information and perform tasks using a tablet or a smartphone. Mobile access offers greater flexibility for users and helps boost overall efficiency and productivity.
Cloud Solutions
Leveraging cloud technologies is critical for automating quality processes. Companies without access to its speed and adaptability will struggle to maintain a competitive edge. MasterControl isn't just a cloud-based solution. It’s dedicated teams and specialized tools to help make your implementation simple and your experience seamless.
Flexible Framework
MasterControl provides an effective framework for a company's quality management system (QMS) by automating all documents- and forms-based processes, connecting all quality processes, and providing a centralized location and single source of truth for all documents and data.
How to Ensure Compliance With Supplement Manufacturing Regulations
The good manufacturing practices (GMP) regulation for dietary supplements, 21 CFR Part 111, mandates proper controls for manufacturing, packaging, labeling, and holding operations. These controls must be meticulously documented. MasterControl's nutraceutical manufacturing software brings automation to the process, keeping your documentation in an audit-ready state and elevating product quality.
Download the white paper
Reasons for Connecting Quality Throughout the Supplement Product Life Cycle
With an integrated QMS that bridges the gap between quality and manufacturing, you can boost efficiencies and enhance product quality across your dietary supplement manufacturing operation. MasterControl's fully connected platform connects crucial processes like document control, training management, and corrective actions, along with batch, calibration, and maintenance records throughout the life cycle of your dietary supplement products.
Download the brochure
Solutions for the
Dietary Supplement Product Lifecycle
Start your dietary supplement or nutraceutical product development on compliant footing with MasterControl Development Excellence. Ensure proper documentation and quality management from day one.
Quality is the top priority throughout the nutraceutical product life cycle. MasterControl Quality Excellence provides automated document control, change control, training management, audit management, corrective action/preventive action (CAPA) management, and unparalleled process connectivity for dietary supplement manufacturing.
Dietary supplement manufacturers are responsible for ensuring quality consistency across their entire supply chain. MasterControl Supplier Excellence helps supplement and nutraceutical manufacturers ensure quality alignment throughout their supplier ecosystems with supplier quality management (SQM), approved vendor lists (AVL), and supplier corrective action requests (SCAR) — all on the same platform.
Dietary supplement and nutraceutical manufacturers often struggle to connect quality processes and manufacturing, and too many production lines still rely on paper. MasterControl Manufacturing Excellence eliminates paper dependency and automates the last mile of the manufacturing production process, crucial for both in-house and contract manufacturing operations.
Once a dietary supplement or nutraceutical product is on the market, manufacturers must continually monitor its performance. MasterControl Postmarket Excellence helps manufacturers track customer complaints and resolve issues efficiently, making it easier for you to maintain product quality and consumer trust.
Resources for Dietary Supplement Manufacturers
Select all the resources you are interested in downloading
GxP Lifeline Blog Posts
Final FDA Rule on Dietary Supplements (21 CFR Part 111) Guidance
In June 2007, the U.S. Federal Drug Administration issued the Dietary Supplement Current Good Manufacturing Practice (CGMP) Final Rule (21 CFR Part 111). In essence, the final rule requires that the proper controls be in place for dietary supplements during manufacturing, packaging, labeling, and holding operations.
Read Blog Post
Top 5 Nutraceutical Trends in 2018 – Functional Foods
The dietary supplement and functional foods markets overlap to a certain extent. Rather than trying to resist this, nutraceutical companies can get the best of both worlds by expanding their offerings to include functional snacks and beverages.
Read Blog Post
Top 5 Nutraceutical Trends of 2019 – Pet Supplements
Supplements aren’t just for people anymore. The pet supplement market has grown with the human supplement market and there’s every indication that it will continue to do so. Taking advantage of this trend involves producing better quality supplements, conducting clinical research, and embracing technology to improve production.
Read Blog Post
Top 5 Nutraceutical Trends: Going Green With Packaging
Plastic is the new GMO. It’s experiencing similar ostracization due to the large amounts of plastic produced each year that winds up in landfills and in the ocean. Moving away from a plastic dependency requires nutraceutical companies to be prepared with innovative ideas and a manufacturing process that is easily adaptable.
Read Blog Post
Case Studies
Eliminating Paper in Dietary Supplement Production to Reduce Errors and Scale Production
Discover how a contract manufacturer of nutritional dietary supplements in liquid and powder form improved its ability to meet demand, shortened a lengthy post-production review process to 72 hours, increased visibility, and reduced time to market by implementing MasterControl solutions.
How Do You Get Quality Experts Around the World on the Same Page?
With 66 global locations, Fagron needed a way to ensure each facility could consistently follow the same quality processes and procedures. Find out why the global leader in pharmaceutical compounding now spends 450 fewer hours per year preparing training materials and how it has improved right-first-time metrics by 100% and reduced deviation times by 50%.
Read the case studyReady to Get Started?
Speak with one of the expert consultants at MasterControl to know how.
