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. 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. 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 Informationsstel le fir Arzneispezialitaten (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 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 -3- 121181118.v1 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.
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”), apply to the sales of the Product in the Nordics, Belgium and the Netherlands, and potentially also for products supplied to the United Kingdom. The Parties shall adhere to the requirements of the Delegated Regulation and Products designated for the respective Territories where Serialization is required and Products shall include a unique identifier and all other mandatory master data as further detailed in the Delegated Regulation (e.g. 2D-Data matrix Code, Human readable). The SUPPLIER shall register and pay any and all fees associated with the Serialization of the Products at the applicable National Medicines Verification Organizations, or equivalent, running the applicable national repositories. Upon reasonable request by SUPPLIER, DISTRIBUTOR shall provide support to SUPPLIER as necessary for SUPPLIER to perform a proper root cause analysis or resolution of possible product falsifications (e.g. in connection with European Medicines Verification System alerts, triggered in the respective Territory, including but not limited to Delegated Regulation countries). The handling of potential falsifications will be further agreed upon in the Quality Agreement.
Serialization. For NATO, there are two acceptable methods or Constructs of serialization:
Serialization. The main dialogue comes up with the seri- alization dialogue, where you input your first name, last name, company and the serial number. This code consists of numbers between 2 and 9 (no ones and no zeros) and all letters between A and Z – except the letters “i” and “o”. Click “Unlock SilverFast” once you have entered all data. SilverFast Product Family The SilverFast product family developed by LaserSoft Imaging AG contains software solutions for the following four application areas: The SilverFast versions are modular. A range of different configuration levels are offered for each area: SE versions for beginners, Ai versions for professionals and Studio versions for expert users.
Serialization. The parties shall cooperate with each other to implement serialization of Product using bi-dimensional codes to allow the tracking of Product from the Facility to United Therapeutics’ end-users. MannKind’s costs of such serialization shall be included in COGs.
Serialization. 7.1 Distributor shall comply with Supplier's serial number format, unless there is written agreement between Supplier and Distributor that supports another format. Distributor shall forward to Supplier for review and acceptance a sample of its serial number format.
