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| S.A.F.E. Info on Allergen Control Programs |
Thanks Emily!!
As part of our overall Allergen Control Program, the following protocols help us to ensure the safety of our products for your family and families like yours:
1. Between each run, batch, or flavor all parts of the processing and bagging equipment are thoroughly cleaned and completely sanitized.
2. To reduce the potential for cross-contamination, we identify allergens throughout the manufacturing process; schedule non-allergen production prior to allergen production runs, minimize traffic of raw materials, packing supplies, and employees during the manufacturing of allergen containing products.
3. Pirate Brands spot checks products for gluten and dairy. (Please note that the facility where our products are made is free of egg, treenut, peanut, fish and shellfish.) We test incoming raw materials and validate our cleaning techniques processing equipment and finished products with a highly sensitive, validated ELISA test.
If you need any additional information, please feel free to contact me.
Emily Anschlowar, MS, RD
Consumer Relations and Regulatory Standards Manager
Pirate Brands
100 Roslyn Ave
Sea Cliff, NY 11579
t: 516.656.4545 x36
C: 516-606-6845
f: 516.656.3079
http://www.piratebrands.com/
ReplyDeleteAny single group must be subjected to the 3 validation cleaning requirement,
except if a rationale is recorded and also approved by the Standard Authority
which the worst-case product of one group is clearly a worst-case product for every one of the groups.
Software validation is a part of the design validation for a finished device,
but is not separately defined in the Quality System regulation.
equipment validation
ReplyDeleteValidation has become one of the pharmaceutical industry’s most recognized and discussed subjects.
It is a critical success factor in product approval and ongoing commercialization.
This article provide brief introduction about the pharmaceutical process validation and its importance according to regulatory provision,
also provide the answer of question like why to do, when to do and how to do it.
This work is to present an introduction and general overview on process validation of pharmaceutical manufacturing process.
Quality is always an imperative prerequisite when we consider any product.
equipment validation
Standard person can validate the Equipment through calibration order.
ReplyDeleteThey will check every the parameters,
Place Heat,humidity & additionally the components changed by maintenance and others.
writing is simply great,thank you for the blog.
equipment validation