Serialization Clause Samples
The Serialization clause establishes that the written contract represents the complete and exclusive agreement between the parties, superseding all prior negotiations, discussions, or agreements. In practice, this means that any previous understandings, whether oral or written, are not legally binding unless explicitly included in the current contract. This clause ensures that only the terms within the signed document are enforceable, thereby preventing disputes over alleged side agreements or prior statements.
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Serialization. SerializationInfoEnumerator respectively its corresponding Contract Wizard class CW_SERIALIZATION_INFO_ENUMERATOR implement Current. However, they do not return an object of type SYSTEM_OBJECT but of type SERIALIZATION_ENTRY. Normally, this is a legal redeclaration since SERIALIZATION_ENTRY is a subtype of SYSTEM_OBJECT. The problem is that SERIALIZATION_ENTRY is expanded and the compiler states a non conforming signature of the redeclaration. Error code: VDRD(2) Type error: redeclaration has non-conforming signature. What to do: make sure that redeclaration uses signature (number and types of arguments and result) conforming to that of the original. Class: CW_SERIALIZATION_INFO_ENUMERATOR Redefined feature: current_: expanded CW_SERIALIZATION_ENTRY From: CW_SERIALIZATION_INFO_ENUMERATOR Precursor: current_: SYSTEM_OBJECT From: IENUMERATOR
Serialization. All Product delivered by Supplier to Lannett shall meet serialization requirements, as outlined in the Drug Supply Chain Security Act (Title II of the Drug Quality and Security Act) signed into law on November 27, 2013. Requirements include, but are not limited to, the addition of Product identifiers imprinted on each sellable unit, on each homogeneous case and on each pallet intended to be introduced in the United States market. Unique product identifiers will include a national drug code, serial identifier (provided by Lannett), lot number, and expiration date. Serial numbers must be aggregated from item to case and case to pallet.
Serialization. As applicable, Buyer will assign serial numbers and Seller will apply to all products accordingly and record serial numbers on all documentation. Assigned serial numbers shall not be altered or replaced and shall remain properly identified for the entirety of Seller’s liability for the parts. If serialization for any product(s) is in question, for any reason, Seller will notify Buyer immediately to determine a resolution.
Serialization. The attributes (axis ranges, colors, text, etc.) and underlying data for graphs can now be saved and restored from a serialization file. The function WGSavePage saves the contents of a page, all graphs within the page, and all objects created in each graph, to a file. The page can be reloaded from the file using the function WGRestorePage. When the WGRestorePage function is called to restore a graph, there is no guarantee that the pointers and handles of the new graph are restored to their original values. All new handles and pointers are allocated when the graph is recreated. The WGSetObjUserID function provides a means of retrieving the handles of the graphical objects in the new, restored graph. This function writes a unique ID to the structure of the specified graphical object. This ID is saved as part of each objects current state when a graph is saved using the WGSavePage serialization function.
Serialization. The Parties agree and acknowledge that the Falsified Medicines Directive (Directive 2011/62/EU) as amended by Directive 2001/83/EC and the European Commission delegated regulation (EU) 2016/161 of 2 October 2015 (“Delegated Regulation”) supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use (“Serialization”), are applicable on the sale and distribution of the Product in the Territory. The Parties shall adhere to the legal requirements applicable in the Territory in connection with Serialization. SUPPLIER shall provide DISTRIBUTOR with Product with a unique identifier, tamper-evident seals and all other mandatory master data as further detailed in the Delegated Regulation (e.g. 2D-Data matrix Code, Human readable). DISTRIBUTOR shall register and pay any and all fees, [***] where necessary, associated with the Serialization of the Product at the German Medicines Verification System (securPharm e.V.), the ACS PharmaProtect GmbH, the Informationsstelle für Arzneispezialitäten (IFA) GmbH and any other relevant agency for Serialization in the Territory, [***]. SUPPLIER or its designated onboarding partner with EMVO (the European Medicines Verification Organisation) shall upload the relevant master data relating to DISTRIBUTOR and its Designated Wholesaler.
Serialization. All deliverable Products shall be serialized with regard to the base part number. No two deliverable Products shall have the same serial number. Serial numbers shall remain the same regardless of configuration changes subsequent to acceptance testing. Serial numbers of Products returned and subsequently not resubmitted shall not be re-assigned.
Serialization. All Product delivered by Seller to Lannett shall meet serialization requirements, as outlined in the Drug Supply Chain Security Act (Title II of the Drug Quality and Security Act) signed into law on November 27, 2013 and provide data to support Product traceability as deemed necessary by Lannett. Requirements include, but are not limited to, the addition of unique Product identifiers Global Trade Item Number (“GTIN”), Serial Number (“SN”), Lot of batch number (“LOT”), expiration date (“EXP”) imprinted on each sellable unit, the same unique Product identifiers mentioned above and Quantity (“QTY”) are required on each homogeneous case and Serialized Shipping Container Code, 18-digit (“SSCC18”) on each pallet intended to be introduced in the US market. Serial numbers must be aggregated from unit to case and case to pallet. Reporting of serial number and aggregation data is required to coincide with finished goods shipment and must conform to data exchange format and connectivity specifications supported by TraceLink. 106569863.v1
Serialization. Supplier shall be responsible for ensuring that the Supply Products are packaged and labelled in accordance with any serialization requirements under Applicable Laws, including, as applicable, under Directive 2001/83/EC as amended and Commission Delegated Regulation (EU) 2016/161. For any Supply Product intended for sale in the EEA, the Parties shall agree in good faith a process for uploading or otherwise providing the serialization data for each pack of Supply Product to the European Medicines Verification System in accordance with Applicable Laws.
Serialization. Serial numbers shall be assigned and permanently attached IAW FAA/DoD(MIL-DTL-18307H) approved procedures.
Serialization. Telechips agrees to comply with Citrix specifications for product serialization as provided and as amended from time to time.