What is cleaning for the Medical Devices and Pharma Industry?
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WHAT IS CLEANING VALIDATION?
WHY CLEANING VALIDATION?
WHEN IS REQUIRED A CLEANING VALIDATION?
HOW TO PREPARE A VALIDATION PROTOCOL IN 24 STEPS?
12 ELEMENTS TO CONSIDER DURING A SUCCESSFUL CLEANING VALIDATION
HOW TO WRITE A CLEANING PROCESS PROCEDURES IN 6 STEPS.
THE TOP ANALYTICAL METHODS USED
PREFERRED TEST METHODS
CONSIDERATIONS TO SELECT THE CORRECT TEST METHOD
TOP CLEANING VALIDATION FACTORS AND LEVELS
ESTABLISHMENT OF ACCEPTABLE CRITERIA
FDA EXPECTATIVE TO CLEANING VALIDATION 21 CFR 211.67
STATUTORY AND REGULATORY REQUIREMENTS
For more details on specific FDA expectations and cleaning definition, follow us
Three (3) options to create a qualification protocol:
Option 1. You can create a great protocol, using a template.
You can download a free sample of a validation template in .pdf format.
To see the complete list of the most popular validation templates, click here.
In addition, you can request a quotation to buy online a full validation template document in MS Word format that is completely editable, ready to fill, and adapt to your needs.
Option 2. We can bring you a formal training on how to create your own validation protocols using our template(s).
This option is recommended if you want to learn more about how to build a robust validation protocol. One of our expert(s) will provide online step-by-step training to your team (unlimited assistance) on how to build a reliable validation protocol using a template. You can improve your corporate validation procedures and policies incorporating our template sections. It includes the template, an exam, and a training certificate for each assistant. Request a quote now.
Option 3. We can create a customized qualification.
One of our expert(s) will create and prepare for you a customized validation protocol with the inputs and specific information of your company. It may include, online support in document creation, execution, or final reporting, Request a quote online.
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PIC/S Guideline to Validation – PI -006-3 (2007)
ICH Guideline Q7 “GMP for APIs
Inspection Guide for Bulk Pharmaceutical Chemicals and the Biotechnology Inspection Guide