At Whistler Technologies, we leverage our extensive knowledge of solventless cannabis extraction to help customers navigate the complexities of GMP regulations. We provide GMP-compliant solventless equipment and guide businesses in establishing solventless processes that are compliant and easy to validate.
By partnering with us you gain:
Our GMP-Driven Design Approach
All of our equipment is designed according to GMP standards, ensuring that every system we build maintains the highest standards of quality, compliance, safety, and cleanliness.
Ra 32
316 Stainless Steel
100% Drainage
No Sharp Corners
No Exposed Threads
Continuous Welds
Good Manufacturing Practices (GMP) regulations ensure the safety and quality of products in industries like pharmaceuticals, food, and packaged goods.
For cannabis extraction facilities, cGMP compliance is crucial for future-proofing operations against regulatory changes, especially for those entering medical markets or exporting products.
Compliance means meeting current standards, preparing for future requirements, equipping your facility with high-quality equipment, and enhancing your reputation for safety and reliability.
Solventless cannabis extraction businesses that value future-proofing and expanding market opportunities will greatly benefit from adhering to GMP standards.
At Whistler Technologies, we employ a 20-point customer plan to ensure we deliver equipment which will adhere to the most stringent GMP standards. This process guarantees that our team understands the scope of customer projects and enables us to identify and resolve any issues during the project delivery.
4. Sales to Engineering hand-off.
5. Customer URS (User Requirement Specification) development and review.
6. Technical design and auxiliary selection review in accordance with URS (User Requirement Specification).
7. Updated solution quotes/pricing (if needed).
8. 3D room design and workflow optimization.
9. Manufacturing kick-off and progress reporting.
10. Qualification document templates.
11. GMP documentation assistance.
12. Quality document collection and consolidation.
13. FAT (Factory Acceptance Testing).
14. Client inspection and sign-off.
15. Passivation and crating.
16. Shipping, import, and insurance assistance.
17. Client inspection after arrival on site.
18. On-site installation, commissioning, and training (on-site aspect optional).
19. On-site validation support (optional).
20. Yield and workflow optimization (recommended 3-6 months after initial start-up).
21. Virtual after-sales technical support and production development assistance.
22. Client feedback, process improvements, and machine upgrades (as available).
The Whistler Technologies team has extensive experience navigating medical cannabis markets and intricate regulatory landscapes. We continuously guide our customers to success, regardless of where their faciliity is located.
The equipment must not have a negative impact on product quality.
The equipment must comply with applicable technical regulations.
The equipment must be suitable for its purpose.
The equipment must be easy to clean.
Whistler Technologies provides you with a comprehensive documentation package, making your GMP validation process simpler.
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