Change Notification Program
- State-of-the-art Management of Changes
- Notifiable Changes
- Change Notification Letters
- How to Receive Change Letters?
- Glossary
Our Life Science business sector serves customers across academia, the biopharmaceutical industry, and the industrial sector, including food & beverage, with a broad portfolio of more than 300,000 products and solutions. To ensure that we provide the most up-to-date product information, we have a best-in-class Change Notification Program based on a compliant Change Control process and on our
M-Clarity™ Program to inform customers about important changes that could impact their R&D or process development programs.
Customer benefits from our Change Notification Program:
- You choose your chemical or consumable product according to the appropriate MQ Quality Segment for your application
- For equipment and spare parts, the EQ and SP Quality Segments reflect controlled requirements
- The amount of information given in the Change Notification is transparent with respect to the Quality Segment of the product
- No more, no less of the information that is required: extensive delineations where necessary, short summary, where sufficient
- Customers define their Change Notification requirements: products on which they would like to receive notifications, persons to be informed, required e-mail or post addresses
- Standardized, easily understandable Change Notification letters and follow-up documentation
State-of-the-art Management of Changes
The process of managing change is complex and includes many deliverables which may occur concurrently or consecutively. Change Control Management is Project Management, and the key requirement is to define tasks, allocate roles and responsibilities, and follow up on tasks in a timely and complete manner. To facilitate Change Control Management and make potential risks, decisions, deliverables, and results transparent, our company uses one of the industry's leading Quality Management software systems, for Change Control. This validated system enables us to initiate, plan, execute, monitor, and control critical processes to guarantee product quality for the benefit of our customers.
We record all changes using our QMS software, and from those changes, we determine if a change notification is required based on the Quality Segment of the product, industry expectations, existing agreements, and the risk assessment associated with the change and its potential impact on the final product and recommended application.
Throughout the Change Notification process, from selecting changes and customers to notify to sending out Change Notification letters, we follow the guidelines from Regulating Authorities and Trade Associations.
Notifiable Changes
Our customers have the option to be informed about relevant changes that might affect the performance of our product and subsequently impact the customer’s processes or products. Change Notifications on one hand, must contain all necessary information, while on the other hand, must be relevant to our customers. Our M-Clarity™ Program ensures we keep this balance and customers get exactly the amount of information needed for the intended use of the product.
The M-Clarity™ Program defines six product Quality Segments from MQ100 to MQ600 for Chemicals and Consumables. For Equipment, the Quality Segments are EQ1 to 4 and for Spare Parts SP1 and SP2. Appropriate Quality Attributes and Notifiable Changes are provided for each segment. According to our M-Clarity™ Program, products with different MQ, EQ, or SP segments get a different extent of change notification.
The Matrix of Notifiable Changes below gives an overview of which information is provided to our customers at each Quality Segment.
Notifiable Changes for Chemicals and Consumables
Notifiable Changes for Equipment and Spare Parts
The Matrix of Notifiable Changes is not intended to be all-inclusive. A Change Team can determine whether a change is notifiable outside of the tables based upon a detailed risk assessment and the recommended use of the product. All Change types relate exclusively to the finished product.
The Explanation of Notifiable Changes explains in depth the notifiable changes at each MQ/EQ/SP segment.
Change Notification Letters
In the event of a change, customers who have entered or “opted-in” to our Change Notification program via a Change Notification Commitment (CNC) or Quality Assurance Agreement (QAA) will be informed via a Change Notification letter driven by the Matrix of Notifiable Changes.
To present the information in the clearest way possible, we use standardized templates for notifications, making it easy to find the details that are most relevant for a customer, regardless of product or manufacturing site.
Our Change Notification letters are individualized to include only the products where we have a customer agreement in place. This eliminates the need to perform comparisons of impacted products to identify those products purchased by our customers.
Our Change Notifications are clear and concise, and set the industry standard. We have developed comprehensive Change Notification letters based on our experience of managing a broad product portfolio, with continuous improvement built-in, based on customer feedback and industry expectations.
How to Receive Change Letters
Change Notification Commitments (CNCs)
The easiest and quickest method to obtain an agreement for Change Notification is to request a product specific agreement via the CNC process. By building our Change Notification program on this opt-in process, we prevent our customers from receiving non-relevant letters as they might trigger unnecessary resource intensive investigations. You can enroll all products deemed critical, despite order history. In setting up a CNC, you choose the products of interest (MQ200 to MQ600, EQ3 and EQ4, SP2) for which you would like to receive Change Notifications, providing the e-mail addresses of departments or individuals to be informed of the change. We do not offer CNCs for products with Quality Segment MQ100, EQ1 and EQ2 or SP1, services, or distributed products.
The term of the CNC is normally five years. Six weeks before the expiry of your CNC, you will receive an expiration notice. With this reminder, you can establish a new CNC to grant continuous Change Notification as necessary or decide against a prolongation. This will prevent receiving change notifications that are no longer relevant.
Quality Agreements (QAAs)
Quality Assurance Agreements are legally binding contracts negotiated between our company and our customers. Having executed a QAA for products used in regulated environments, you can be sure to comply with applicable regulatory and legal requirements.
QAAs address and define various topics related to the quality standards/systems/ services applicable to the covered products: Quality Management System standards/certifications (i. e., pharmaceutical GMP, ICH Q7, IPEC PGQ GMP, ISO-9001, ISO-13485, ISO-22000), complaint handling, audits, recalls, documentation support, level of verification/validation, and notification of changes. Due to the extended requirements and support levels that need to be in place, QAAs are available for products with MQ segments of MQ300 and above.
The term of a QAA is five years. An expiry notice will be received two months in advance, to allow time to prepare for renewal.
When the QAA is finalized and fully signed, the information is secured in our dedicated IT system. Change Notifications will be received for the products covered by the QAA in accordance with the M-Clarity™ program.
If you are interested in a QAA or a CNC for critical raw materials, please contact your local representative.
Change Notification Glossary |
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