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    All global serialisation requirements at a glance - compact and comprehensible

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    Countries

    61

    Deadlines

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  • OCS-Webinars for your competitive edge

    Benefit from our competence and passion. Secure your marketability with the knowledge to give you the upper hand. OCS provides innovative solutions that are sure to impress.

    Check out our past webinar:

    The clock is ticking: How important are global serialisation obligations for the pharmaceutical industry?

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    TQS – LE SYSTÈME TRACK & TRACE OPTIMAL POUR LA SÉRIALISATION GLOBALE

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    Partenaire GS1 et membre du groupe de travail SCS

    Un service après-vente exceptionnel

    Le compte à rebours a commencé !

    Contactez nos spécialistes de la sérialisation afin d’obtenir leur support pour le déploiement de la directive Européenne sur les médicaments falsifiés.

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    Une traçabilité sans faille pour des médicaments sûrs

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    Le compte à rebours a commencé pour la directive UE

    Sérialisez MAINTENANT!

Opportunités et risques liés à la mise en œuvre de la directive Européenne « Médicaments Falsifiés »

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Carte du monde TQS
Nos experts en sérialisation vous proposent un condensé d'informations facile à comprendre comportant toutes les données pertinentes telles que les directives nationales contre la falsification des produits pharmaceutiques, les exigences fondamentales relatives au marquage, les délais de mise en œuvre et les analyses des situations du marché en termes de développements futurs. Vous trouverez tout cela sous forme interactive et clairement structurée dans la carte du monde TQS. Cliquez tout simplement sur le pays de votre choix pour obtenir toutes les données pertinentes.

European Union

Regulation Name / Authority

Directive 2011/62/EU / EU Commission

Serialisation Serialisation

Deadline

February 09, 2019

Data Carrier

Data Matrix ECC200

Data Elements

Unique product identification number (e.g. GTIN/NTIN/PPN), Batch/Lot number, Expiry date, Serial number, National reimbursement number (if applicable).

Tamper Evident

Yes

Aggregation Aggregation

Deadline

Not mandatory

Expert View

Even if the European Falsified Medicine Directive (FMD) is an end-to-end system, the wholesalers and hospital pharmacies will claim for aggregation. This will allow the wholesaler to easily meet the risk-based verification approach if cases or even pallets of the related products are not directly supplied from a manufacturing or marketing authorization holder (or a person supplying on their behalf) and if the product is returned by another wholesale distributor or a pharmacy. Aggregation will also allow the hospital pharmacies to easily decommission their incoming shipments in cases or even pallets.


Belgium

Regulation Name / Authority

APB (Belgian Pharmaceutical Association) / Belgian MoH

Serialisation Serialisation

Deadline

Jul 01, 2004

Data Carrier

Code 128 C on Vignette

Data Elements

7-digit national registration number (CNK) + Unique 8-digit serial number + 1 control digit

Tamper Evident

No

Aggregation Aggregation

Deadline

Not mandatory

Expert View

Until the EU Falsified Medicine Directive is not implemented, all products in Belgium need to be labeled with the vignettes. As Belgium has +6 years more time for the implementation (Feb 09, 2025), labeling equipment will be mandatory for the time being.


France

Regulation Name / Authority

CIP (Club Inter Pharmaceutique) - / ANSM (French National Agency for Medicines and Health Products Safety)

Batch Coding Batch Coding

Deadline

January 01, 2011

Data Carrier

GS1 Data Matrix ECC200

cip13code

Beispielcodierung

Data Elements

Unique product identification number (French CIP code / NTIN) - (AI 01), Expiry date (AI 17), Batch/Lot number (AI 10).

Serialisation Serialisation

Deadline

Not mandatory

Tamper Evident

No

Aggregation Aggregation

Deadline

Not mandatory

Expert View

Until the EU Falsified Medicine Directive is not implemented, all products in France need to be batch coded according to CIP guideline.


Germany

Regulation Name / Authority

NMVS (National System according to EU FMD) - ACS-MAH-System “securPharm”

Serialisation Serialisation

Deadline

February 09, 2019

Data Carrier

Data Matrix ECC200 (ASC/IFA- or GS1-Format)

Data Elements

Unique product identification number (PPN or NTIN), Batch/Lot number, Expiry date, Serial number.

Tamper Evident

Yes

Aggregation Aggregation

Deadline

Not mandatory

Expert View

securPharm is the National Medicines Verification System (NMVS) of Germany. Since 2013, pharmaceutical companies are able to use securPharm and practice their own processes. As such, it serves as a partner within the safety network in Europe provided by the European Medicines Verification Organisation (EMVO). In the Delegated Regulation the national reimbursement number is mentioned. For pharmaceuticals destined for the German market, it is included in the product code in form of the PZN and therefore does not need to be listed as a separate fifth element pursuant to Article 4 (e) of the Delegated Regulation.


Greece

Regulation Name / Authority

Greek Ministry of Health & Welfare

Serialisation Serialisation

Deadline

Apr 08, 2004

Data Carrier

Code 128 and EAN-13 on Vignette

Data Elements

Serial number (in Code 128) and Greek EOF code (9 digits) incl. NPO registration number (in EAN-13)

Tamper Evident

No

Aggregation Aggregation

Deadline

Not mandatory

Expert View

Until the EU Falsified Medicine Directive is not implemented, all products in Greece need to be labeled with the respective vignettes. This sticker is issued by EOF (“Ethnikos Organismos Farmakon” / National Organisation for Medicines) free of charge to companies. It is produced by a special aquarelled paper incl. the national emblem and the name of EOF (solely visible by UV). The sticker is 27 x 24mm and contains (typed by EOF): name of the company, production year and sticker number. The manufacturer is obliged to type the following: product name, pharmaceutical form and strength, code number (assigned by EOF and unique to the product) and the retail price. As Greece has +6 years more time for the implementation (Feb 09, 2025), labeling equipment will be mandatory for the time being.


Italy

Regulation Name / Authority

“Italian Bollini” / Italian MoH

Serialisation Serialisation

Deadline

Jan 04, 2005 “old Bollino” / Dec 31, 2015 “new Bollino”

Data Carrier

2 linear barcodes (Code 39 and ITF) on Bollino (Vignette)

Data Elements

“Old Bollino”: National market authorisation code (AIC), Serial number; “New Bollino”: 3 barcodes: 2 linear barcodes (Code 39 and ITF) encoding the AIC code and the serial number and a 2D DataMatrix encoding the AIC and the serial number.

Tamper Evident

No

Aggregation Aggregation

Deadline

Not mandatory

Expert View

Until the EU Falsified Medicine Directive is not implemented, all products in Italy need to be labeled with the “New Bollini” vignettes. As Italy has +6 years more time for the implementation (Feb 09, 2025), labeling equipment will be mandatory for the time being.

Argentina

Regulation Name / Authority

ANMAT drug traceability system / Administración Nacional de Medicamentos, Alimentos y Tecnología Médica

Serialisation Serialisation

Deadline

Aug 30, 2015 (and several for selected products before)

Data Carrier

GS1 Data Matrix ECC200, GS1 128, RFID tag

gs1DataMatrix

Beispielcodierung

Data Elements

GTIN (AI 01), Serial Number (AI 21)

Tamper Evident

No

Aggregation Aggregation

Deadline

Not mandatory

Expert View

„The regulation Disposición 963/2015 on traceability, released by ANMAT on January 30, 2015, expended the scope and the specifications of the drug traceability system. Since then, the drugs also have to be marked with lot number and expiry date (format (DD/MM/YY or DD/MM/YYYY). Deadline for implementation of these requirements was March 02, 2015.“

Brazil

Regulation Name / Authority

SNCM “Sistema Nacional de Controle de Medicamentos” Law No. 11.903/2009 / ANVISA

Serialisation Serialisation

Deadline

Under discussion

Data Carrier

Data Matrix ECC200

Data Elements

GTIN (AI 01) or National Number (NHRN) - (AI 713), Expiration Date (AI 17), Batch/Lot Number (AI 10), Serial Number (AI 21)

Tamper Evident

No

Aggregation Aggregation

Deadline

Under discussion

Data Carrier

Possibly GS1 128

Data Elements

Possibly SSCC (AI 00)

Expert View

GS1 standards are not a regulation requirement in Brazil. But as the usage of a GTIN, the data carries GS1 Data Matrix, GS1 128 and SSCC are market recommendations. There is a requirement for secondary packaging, that manufacturing date needs to be printed solely in clear text (Regulation RDC 71). The deadline for serialization and tracking for all pharmaceuticals is still in force.

China - Human

Regulation Name / Authority

CFDA Decree No.28 / “National e-coding system” / CFDA

Serialisation Serialisation

Deadline

Dec 31, 2015 - ON HOLD since Feb 20, 2016

Data Carrier

Linear Code 128 C

code128c

Beispielcodierung

Data Elements

NATIONAL product code (country number, drug category number, drug identification number and the check number (14 digits))

Tamper Evident

No

Aggregation Aggregation

Deadline

Dec 31, 2015 - ON HOLD since Feb 20, 2016

Data Carrier

Linear Code 128 C

Data Elements

NATIONAL product code (country number, drug category number, drug identification number and the check number (14 digits))

Expert View

Even if CFDA announced the suspension of the implementation of relevant provisions on drug electronic supervision, most companies still follow the regulation. GS1 wrote a recommendation letter to advocate for the usage of GS1 standards. New GSP (Good Supply Practice) regulation has been released, but new deadlines are still missing.

China - Veterinary

Regulation Name / Authority

Ministry of Agriculture of the People’s Republic of China

Serialisation Serialisation

Deadline

Jun 30, 2016

Data Carrier

QR Code (UTF-8)

Data Elements

Veterinary drug product tracing code (24-digit number randomly generated by the national veterinary drug product tracing system) containing tracing code, product name, product approval number or registration certificate number of import veterinary drugs, abbreviation of the manufacturing enterprise and contact telephone

Tamper Evident

No

Aggregation Aggregation

Deadline

Not mandatory

Expert View

If the uniform veterinary drug two-dimensional code marks cannot be printed on the minimum sales package on the products due to the limitations of the package size for the products with special circumstances such as ampoules, vials less than 5 ml or irregular shaped bottles, the uniformly marked veterinary drug two-dimensional code should be printed on the package of the upper level on the minimum sales package. The specific products should be applied by the manufacturing enterprises of the veterinary drugs, reviewed and confirmed by the Veterinary Bureau of the Ministry of Agriculture.

India

Regulation Name / Authority

DGFT (Directorate General of Foreign Trade)

Primary Level Packaging

Serialisation Serialisation

Deadline

Apr 01, 2015 (solely mono-cartons); Remaining delayed until further notice

Data Carrier

EAN/UPC or GS1 Data Matrix ECC200 or GS1 128 or GS1 DataBar

Data Elements

GTIN (AI 01), Batch/Lot Number (AI 10), Expiration Date (AI 17) and Serial Number (AI 21)

Tamper Evident

No

Secondary Level Packaging

Serialisation Serialisation

Deadline

Oct 01, 2013

Data Carrier

GS1 Data Matrix ECC200 or GS1 128 or GS1 DataBar

gs1DataMatrix

Beispielcodierung

Data Elements

GTIN (AI 01), Batch/Lot Number (AI 10), Expiration Date (AI 17) and Serial Number (AI 21)

Tamper Evident

No

Aggregation Aggregation

Deadline

Oct 01, 2013

Data Carrier

GS1 Data Matrix ECC200 or GS1 128 or GS1 DataBar

Data Elements

GTIN (AI 01), Batch/Lot Number (AI 10), Expiration Date (AI 17) and Serial Number (AI 21)

Tertiary Level Packaging

Serialisation Serialisation

Deadline

Oct 01, 2011

Data Carrier

GS1 128 or GS1 Data Matrix ECC200 (first code) / GS1 128 (second code)

gs1DataMatrix

Beispielcodierung

Data Elements

a) Shipping cases: First code – GTIN (AI 01), Batch/Lot Number (AI 10), Expiration Date (AI 17) and Serial Number (AI 21) // Second code – SSCC (AI 00);

b) Pallets: SSCC (AI 00)

Tamper Evident

No

Expert View

Pharmaceutical manufacturers exporting medicines, need to follow the DGFT regulation. On Jan 05, 2016, the Indian DGFT has released the Public Notice 52/2015-2020. Primary level is still exempted from labelling with a 2D barcode. The data elements can optionally be printed in human readable format on primary level. However, this information needs to be provided to the DAVA portal, as the system requires its input and doesn’t except empty fields. In case having no “real” primary level data elements available, some “virtual” information needs to be provided. This “virtual” information set needs to be maintained by the manufacturer.

Iran

Regulation Name / Authority

TTAC Executive guideline No. 660/11873 dated Sept. 7, 2014

Serialisation Serialisation

Deadline

Jan 01, 2015

Data Carrier

GS1 Data Matrix

gs1DataMatrix

Beispielcodierung

Data Elements

GTIN (AI 01), Serial Number (AI 21), Batch/Lot Number (AI 10), Expiration Date (AI 17)

Tamper Evident

No

Aggregation Aggregation

Deadline

Not mandatory

Expert View

The GS1 Data Matrix and the originality number* in coated form will be in a specified place measuring 20 by 40 mm, with a white background and yellow margin. The UID is required to be a 20 digit number, whereas the first 4 or 5 digits of the UID identify the company generating the UID and the remaining numbers are randomly generated.

*In addition to GTIN, UID, Lot and Exp, a 16-digit number will be printed under the scratch label for the patient or end user to use for authentication purposes.

Jordan

Regulation Name / Authority

Guidelines of Identification and Bar coding of Medicinal Products for Human Use / JFDA

Batch Coding Batch Coding

Deadline

Jul 01, 2018

Data Carrier

GS1 Data Matrix

cip13code

Beispielcodierung

Data Elements

GTIN (AI 01), Expiration Date (AI 17), Batch/Lot Number (AI 10)

Serialisation Serialisation

Deadline

2020 (To be decided)

Data Carrier

GS1 Data Matrix

gs1DataMatrix

Beispielcodierung

Data Elements

GTIN (AI 01), Serial Number (AI 21), Expiration Date (AI 17), Batch/Lot Number (AI 10)

Tamper Evident

No

Aggregation Aggregation

Deadline

Not mandatory

Expert View

In human readable format, it is sufficient to print the GTIN close to the GS1 Data Matrix, if the expiration date and batch number are found elsewhere on the pack.

Philippines

Regulation Name / Authority

Guidelines on Implementing FDA Circular No. 2014-011

Batch Coding Batch Coding

Deadline

Jun 30, 2016 - ON HOLD

Data Carrier

Linear code or Data Matrix (possibly GS1)

Data Elements

GTIN (AI 01) , Expiration Date (AI 17), Batch/Lot Number (AI 10)

Serialisation Serialisation

Tamper Evident

No

Expert View

The policy “Unique Global Product Identification Number for Drug Products'‘ requires the use of their so called “Global Product Identification Number” (GPIN) for drug products (which is a unique 14-digit code specific for a product presentation of a specific company that is secured from a global standards organization – similar to a GTIN), the batch number and expiry date. Since Jul 25, 2016 the implementation requirement is on hold.

Russia

Regulation Name / Authority

Federal Law № 61-FZ "Circulation of Medicines" / Federal Service for Surveillance in Healthcare

Serialisation Serialisation

Deadline

Jan 01, 2017 (selected products); Jan 01, 2018 (essential list); Jan 2019 (other drugs)

Data Carrier

Data Matrix (possibly GS1 - To be decided)

Data Elements

Country of manufacture, the manufacturing company, batch number, expiry date, and an unique identifier (TBD)

Tamper Evident

No

Expert View

The first deadline of the FGIS MDLP (Federal Public Information System for Monitoring the Movement of Drugs) concerns products related to hemophilia, cystic fibrosis, pituitary dwarfism, Gaucher's disease, malignant neoplasms of lymphoid, hematopoietic and related tissue, multiple sclerosis and those after transplantation of organs and/or tissues. Pilot by federal MoH planned with deadline for Oct 31, 2016. The scope contains (a) no less than one local, and one foreign producer; (b) no less than one pharmacy having several sales outlets in Moscow, Moscow region, and Saint Petersburg; (c) medical institutes which are treating patients with 7N diseases.

Saudi Arabia

Regulation Name / Authority

Guidance for the industry on Saudi Drug Code (SDC) and drug barcoding specifications / Saudi FDA

Batch Coding Batch Coding

Deadline

Mar 21, 2015

Data Carrier

GS1 Data Matrix ECC200

cip13code

Beispielcodierung

Data Elements

GTIN (AI 01), Batch/Lot Number (AI 10), Expiration Date (AI 17)

Serialisation Serialisation

Deadline

Mar 12, 2017

Data Carrier

GS1 Data Matrix ECC200

gs1DataMatrix

Beispielcodierung

Data Elements

GTIN (AI 01), Serial Number (AI 21), Batch/Lot Number (AI 10), Expiration Date (AI 17)

Tamper Evident

No

Aggregation Aggregation

Deadline

Not mandatory

Expert View

In the first draft regulation, SFDA was claiming for the coding of the pack size. Since Jul 07, 2014 this obsolete as a GTIN is already providing the pack size information.

South Korea

Regulation Name / Authority

Korean Pharmaceuticals Information Service / Ministry for Food and Drug Safety (MFDS - formely Korean FDA)

Batch Coding Batch Coding

Deadline

Jan 01, 2010 (solely KDC coding); Jan 01, 2012 (specific products); Jan 01, 2013 (all Rx products)

Data Carrier

GS1 Data Matrix ECC200 or GS1 128

cip13code

Beispielcodierung

Data Elements

KDC (Korean Drug Code / NTIN) - (AI 01), Expiration Date (AI 17) and Batch/Lot Number (AI 10)

Serialisation Serialisation

Deadline

Jan 01, 2015 (selected products); Jan 01, 2016 (all products)

Data Carrier

GS1 Data Matrix ECC200 or GS1 128 or RFID

gs1DataMatrix

Beispielcodierung

Data Elements

KDC (Korean Drug Code / NTIN) - (AI 01), Serial Number (AI 21), Batch/Lot Number (AI 10), Expiration Date (AI 17)

Tamper Evident

No

Aggregation Aggregation

Deadline

Not mandatory

Expert View

Reporting transition period of 6 months to Jul 01, 2016. Even if aggregation is not mandatory until now, all producers are already using aggregation systems for convenience during warehousing / release.

Taiwan

Regulation Name / Authority

Taiwan Food and Drug Administration (TFDA)

Batch Coding Batch Coding

Deadline

Jan 01, 2018 (for secondary and tertiary level)

Data Carrier

GS1 Data Matrix ECC200 (secondary) / GS1 Data Matrix ECC200 or GS1 128 (tertiary)

cip13code

Beispielcodierung

Data Elements

GTIN (AI 01), Batch/Lot Number (AI 10) and Expiration Date (AI 17)

Serialisation Serialisation

Deadline

Jan 01, 2019 (for secondary and tertiary level)

Data Carrier

GS1 Data Matrix ECC200 (secondary) / GS1 Data Matrix ECC200 or GS1 128 (tertiary)

gs1DataMatrix

Beispielcodierung

Data Elements

GTIN (AI 01), Serial Number (AI 21), Batch/Lot Number (AI 10) and Expiration Date (AI 17)

Tamper Evident

No

Aggregation Aggregation

Deadline

Jan 01, 2020

Expert View

The requirements on primary level packaging have been removed.

Turkey

Regulation Name / Authority

“Regulation Regarding the Packaging and Labeling of Medicinal Products for Human Use” Official Gazette 25904 from 12/08/2005 – İTS „ilaç takip sistemi“ / Turkey MoH

Serialisation Serialisation

Deadline

Jun 01, 2010

Data Carrier

GS1 Data Matrix ECC200

gs1DataMatrix

Beispielcodierung

Data Elements

GTIN (AI 01), Serial Number (AI 21), Expiration Date (AI 17), Batch/Lot Number (AI 10)

Tamper Evident

No

Aggregation Aggregation

Deadline

Jun 01, 2010

Data Carrier

GS1 128

Data Elements

SSCC (AI 00)

Expert View

Turkey requires full aggregation. So also bundles, shipping cases and pallets need to be serialized. These packaging levels are called transportation units and are numbered using the SSCC (Serial Shipping Container Code).

USA

Regulation Name / Authority

Drug Quality and Security Act (HR 3204) - Title II: Drug Drug Supply Chain Security Act (DSCSA) / US FDA

Serialisation Serialisation

Deadline

Nov 27, 2017

Data Carrier

Data Matrix ECC200

Data Elements

GTIN (AI 01), Serial Number (AI 21), Expiration Date (AI 17) and Batch/Lot Number (AI 10)

Tamper Evident

No

Aggregation Aggregation

Deadline

Nov 01, 2023 (To be decided)

Data Carrier

To be decided

Data Elements

To be decided

Expert View

Even if aggregation is not mandatory until now, the “big 3 wholesalers” already claimed for using aggregation systems and to follow the HDMA guidelines. They wrote a letter to all their customers (pharmaceutical manufacturers).

Infographie TQS

Toutes les exigences globales de la sérialisation en un coup d'œil – une présentation concise et facile à comprendre. Vous pouvez télécharger l'infographie TQS au format PDF, l'imprimer et même la distribuer.

Télécharger l'infographie

Avec TQS, OCS Checkweighers dispose d'un système Track & Trace souple et modulaire ayant été parfaitement adapté à nos besoins. […] Avec TQS, nous sommes parfaitement armés pour répondre aux futures exigences globales imposées par les solutions Track & Trace.

Dr. Marco Klingele | Track & Trace Program Lead / Head of Administration | Losan Pharma GmbH

[…] Grâce à ConfigureFast, l'interface utilisateur entièrement intégrée, il n'est plus nécessaire de configurer séparément les différentes mises en page d'impression et le système de traitement d'image dans tous les systèmes TQS, ce qui constitue un avantage majeur. Il en résulte des temps de configuration extrêmement courts et par conséquent une productivité nettement plus élevée dans la ligne.

Alexander Pohl | Technical Expert Packaging | Aenova-Group

Avec TQS, nous sommes parfaitement armés pour une sérialisation continue et une agrégation complète.En ce qui concerne surtout les futures exportations vers les pays d'Extrême-Orient, la qualité et la flexibilité de notre système extrêmement compact nous permettent d'apporter la réponse parfaite à toutes les dispositions d'étiquetage prévues à l'échelle internationale.

Jürgen Back | Packaging Production Engineer | MEDA Manufacturing GmbH

Vos avantages en un coup d’œil
OCS Checkweighers est non seulement fournisseur de solutions chez GS1 Germany mais aussi membre votant du GS1 Global Healthcare User Group. Nous travaillons en collaboration avec les plus grands fabricants de médicaments et mettons immédiatement en application les spécifications et modifications pertinentes relatives à la sérialisation et à l'agrégation.

Membre de l'Open SCS Working Group, OCS Checkweighers se bat pour des options flexibles intégrables dans des infrastructures de production déjà existantes mais aussi pour un concept de connectivité ouvert et standardisé avec des systèmes de niveau supérieur.

OCS est favorable à une norme industrielle améliorée plutôt qu'à des solutions autarciques propriétaires encore trop souvent utilisées actuellement. En particulier la dépendance artificielle de nombreux fournisseurs entraîne tôt ou tard des problèmes de disponibilité très dangereux. Chaque fabricant de médicaments doit être indépendant et doit pouvoir choisir librement son équipement.

Les solutions de triage pondéral et d'inspection rapides et ultra précises proposées par OCS Checkweighers pour le contrôle qualité, constituent depuis plus de 20 ans un standard fiable dans les lignes de production des plus grands fabricants de l'industrie pharmaceutique, cosmétique, alimentaire et chimique.

Sur la base des expériences faites avec des applications hightech individuelles et dans l'optique de la future obligation de sérialisation pour les médicaments délivrés sur ordonnance, OCS Checkweighers a complété sa gamme de produits par le Traceable Quality System (TQS), la solution Track & Trace qui connaît un vif succès.

TQS est synonyme de sécurité maximale, d’utilisation ultra simple et offre à tous les fabricants de produits pharmaceutiques une solution personnalisée et adaptée pour la sérialisation et l'agrégation de préparations médicamenteuses. La commande des unités fonctionnelles, le convoyage des produits, le marquage et l’inspection par caméra est effectué de manière totalement intégrée et en toute simplicité à partir d'un seul logiciel.

OCS Checkweighers accorde une attention particulière au développement de toutes les techniques requises ainsi qu'à la fabrication de tous les composants principaux dans ses propres établissements. Il en résulte un niveau de création de valeur exceptionnel qui nous permet d'être en grande partie indépendants des fournisseurs et de livrer en respectant les délais.

Chez OCS Checkweighers, le développement, la construction et la fabrication sont réunis sous un même toit. Cette philosophie garantit une flexibilité maximale dans la réalisation de chaque configuration de produit individuelle.

En tant que client d'OCS Checkweighers, vous bénéficiez de notre réseau de services international. Nous vous apportons notre aide pour mettre en œuvre votre solution TQS personnalisée, restons à votre disposition pour initier et former vos opérateurs ainsi que pour effectuer la maintenance préventive des installations.

Nous nous ferons un plaisir de vous conseiller au cours d'un rendez-vous personnalisé pour vous informer sur l'étendue et la réalisation des différentes prestations.

Des médicaments sûrs constituent un bien précieux garantissant, dans les moments difficiles, la survie de chaque être humain. Loin de toute considération économique, cet objectif donne naissance à une responsabilité purement éthique visant à n'épargner aucun effort pour mettre fin à la falsification des médicaments dans le monde entier. OCS Checkweighers se fait un grand plaisir de relever ce défi ambitieux dans un souci d'offrir aux consommateurs la meilleure protection possible.

Des fabricants de médicaments et des sous-traitants renommés comptent déjà parmi nos clients exigeants. Track & Trace vous intéresse ? Alors n'hésitez pas à nous contacter. Nous ferons de notre mieux pour vous aider.

Profitez de cette opportunité ! Sérialisez vos produits maintenant !

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