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 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. 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. 7.1 Marketing Authorization Holder will be responsible and bear the costs for the implementation of the Falsified Medicines Directive (Directive 2011/62/EU) and the new delegated act on the safety features (Commission Delegated Regulation (EU) 2016/161 - "the Delegated Regulation") that may impact on the product information and the marketing authorization dossier. In particular, placing of safety features, a unique identifier (UI) carried by a 2-D barcode and an anti-tampering device (ATD), on the packaging of prescription medicines and certain non-prescription medicines for the purposes of authentication and identification. In addition, the Marketing Authorization Holder will be responsible of uploading the UI of the units marketed in the EU into the correspondent national repository called National Medicine Verification Systems (“NMVS”) that will be connected to the centralized European Medicine Verification System (“EMVS”).
Serialization. Contractor’s requests for serial number assignment shall be sent to the following e-mail address: XXXX_XXXXXXxxxxx.xxx@xxxx.xxx. 3.0 QUALITY ASSURANCE PROVISIONS
Serialization. When launching SilverFastPrinTao for the first time, the serialization dialogue will appear. Enter your name, company and the SilverFastPrinTao serial number. Please ensure that you are logged into the PC/Mac with administrator rights. The serial number is a 30 digit code, consist- ing of 6 groups with 5 digits each. This code consists of numbers between 2 and 9 (no ones and no zeros), and all let- ters between A and Z – except the letters “i” and “o”.
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. The installations CD/DVD must be in the optical drive before and during this step. SilverFast Product Family The SilverFast product family developed by LaserSoft Imaging AG contains software solutions for the following four application areas: Scanning Optimization of scan- ner raw data Digital camera Printing 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. Serial numbers shall be assigned and permanently attached IAW FAA/DoD(MIL-DTL-18307H) approved procedures.
