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3.2 billion

3.2 billion

vaccines transported in our packaging each year

250,000

250,000

shipping units produced annually

4 separate companies

4 separate companies

within the Sofrigam Group

18,000 m2

18,000 m2

used solely for the manufacture of packaging

40 years

40 years

of innovation and performance

History

Our Mission

Environmental policy

Quality policy

Sofrigam Group

Recruitment

History

Our Mission

Help you to heal the world

Our aim is to help you to improve the efficacy of medicine by facilitating the movement of your innovations more easily around the world.

Our mission has two objectives :

  • to maintain your products at perfectly stable temperatures throughout their shipment;
  • to help you improve your logistics chain.

We offer our our expertise, acquired over 40 years’ of experience, alongside the most important contacts in the health field to help you reduce your logistic costs and to minimise your environmental footprint – while simultaneously meeting the regulatory requirements in the cold chain transport of pharmaceutical products.

Environmental policy

OUR COMMITMENT TO THE ENVIRONMENT IN A FEW FIGURES:

36 TONNES OF RECYCLED WASTE RE-USED EACH YEAR

25 % REDUCTION OF WASTE IN 2019

10 % OF GREEN ENERGY PRODUCED BY THE WIND TURBINE AT OUR PRODUCTION SITE
THE ENVIRONMENT: MORE THAN JUST A COMMITMENT, IT IS A COURSE OF ACTION

Quality policy

Your level of standards is ours

Every day we work with our collaborators, partners and suppliers to ensure maximum customer satisfaction in terms of quality control and time scales, constantly seeking improvements in our methods.

Sofrigam will help you protect the integrity of your high value-added products without the need to compromise.

All our solutions meet the European directives in Good Distribution Practice guidelines (GDP), the object being to guarantee the quality and integrity of the health products at all levels in the distribution circuit. This requires an on-going, rigorous reviewing process in terms of our partners and suppliers to confirm that they maintain our values and standards of quality.

Our quality policy in a few figures:

94% of OTIF (On Time In Full) FOR THE LAST 5 YEARS

511,180 TESTS ON FINISHED PRODUCTS

38 QUALITY CONTROL POINTS VERIFIED PER PRODUCT

 

13,296 RAW MATERIALS VERIFIED

18 CLIENT AUDITS

OUR CERTIFICATIONS DEMONSTRATE OUR TRUE COMMITMENT

Our Quality Management is certified ISO 9001 and reflects two main commitments: client satisfaction and continual improvement. We are establishing a system to constantly seek to improve the manufacturing process of our packaging as well as monitoring client satisfaction. Our Quality Management system is regularly audited by the organisation that issues the ISO certificates and is followed closely by our pharmaceutical clients.

Additionally, our Environmental Management is certified ISO 14001. To validate our guarantee of regular improvement in environmental performance as well as controlling our energy expenses, we confirm that at all times we follow a policy of continuous improvement to reduce our environmental footprint in the short, medium and long term, as well as limiting our energy expenses.

>>> Consult our Quality and Environmental Policy

Sofrigam Group

THE STRENGTH OF AN INTERNATIONAL GROUP

THE STRENGTH OF AN INTERNATIONAL GROUP
THE STRENGTH OF AN INTERNATIONAL GROUP

Sofrigam is now an international group, comprising of companies meeting the needs of the cold chain management throughout the whole pharmaceutical supply chain, from the production of medication to last-mile logistics.

Sofrigam designs and develops cold chain management solutions (containers, packaging, bags and pouches) for pharmaceutical, biotechnological and chemical companies.

Initially specialising in passive packaging, today Sofrigam has turned towards active, innovative technologies with Coldway Technologies. The synergy between the technical nature of the Sofrigam and the Coldway Inside° technology –  a production system of autonomous thermic energy – represents a major innovation in the field of cold production and storage.

Those who are involved with the last-mile logistics – in either the health field or the food industry –  will be interested in La Boutique du Froid (The Cold Shop), an on-line platform with experts available to assist you to seek cold chain management solutions. All the recommended pathways suggested by members of the Sofrigam Group are tested, pre-qualified and validated by the thermal testing laboratory Ater Métrologie, to ensure their reliability and performance according to the norms and regulations in force.  

 

Recruitment

Sofrigam is regularly looking for new talent. Do you want to bring new perspectives to your career? Would you like to participate in the development of a dynamic and innovative company with an international reputation? Join our teams!

  • Sofrigam Group
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Sofrigam
Coldway Technologies
ColdShop
Ater Metrology
Partners
Competence Certificate – examining the impartiality and the independence of a certifying body, according to the norms in force. Through accreditation, an authoritative body formally recognises that an organisation or individual is competent to carry out certain tasks. Accreditation establishes a large degree of confidence in the body’s ability to issue certifications, representing confirmation from the relevant organisation. The certificates, delivered by those accredited to do so, are thereby endowed with complete trust and credibility on the market.
Crate or insulated container equipped with the Coldway Inside° refrigeration production system (usually in the upper part).
Insulated mobile crate equipped with Coldway Inside° refrigeration system (in its lower part).
The title of this regulatory reference is: ‘Guidelines of 5 November 2013 on Good Distribution Practice of medicinal products for human use’ (2013/C 343/01). This document is issued by the institutions, bodies and organisations from within the European Union. It fixes the rules in respect of the distribution of medication (storage, transport, sub-contracting, etc.).
CertiCold is a quality label for cold chain products delivered on the basis of private technical specifications and established in conjunction with the relevant manufacturers and the professional users. The label CertiCold Pharma relates to cold chain equipment for health products – for packaging solutions for the transportation of health products and for transport units under controlled temperature for health products.
Procedure by which a third part gives written assurance that a product, process or service conforms to specified requirements.
This is the full method used to maintain a product at a constant temperature throughout the transport process, all the way to its final destination.
An autonomous, active refrigeration system using the technology patented by Coldway Technologies. The Rolls and active Containers are all equipped with this technology, facilitating constant and controlled refrigeration which is both silent and de-carbonised.
This is a measuring device which records and stores temperature readings. It is equipped with a temperature probe, memory storage, a display system and alarms. Some recorders can also communicate the results in real-time.
Packaging case (or box or container) comprising of a thermal insulation on each wall to reduce heat exchange with the environment.
Insulated box equipped with a refrigeration source (refrigeration accumulators). The refrigeration source may be eutectic plates or phase-change materials (PCM) or even dry-ice.
The pharmaceutical supply chain from start to finish, or End-to-End, involves the logistical operations of transporting and storing medication, from the manufacturing site to delivery at the health facilities such as clinics, hospitals, and dispensaries – and in some cases even to the patient himself.
The eutectic plates are water-based thermic accumulators (for cold or heat). The aqueous solution facilitates the stocking of thermic energy in the solid or liquid sensitive phase and by the changing of the solid/liquid phase. With fusion temperatures below or equal to 0 °C, the eutectic plates permit the maintenance of temperature differences between +2/+8 °C, under -5 °C, under -15 °C, under -18 °C or even under -20 °C.
A characteristic of a material represents its aptitude to accumulate a greater or lesser amount of heat for a given variation in temperature. The thermal inertia of a material depends on its density, thermal conductivity and mass heat.
This material is characterised by its low thermal conductivity. The most commonly used insulating materials in the manufacture of isothermal packaging are: - Polystyrene – the traditional thermal insulator whose thermal conductivity varies between 0.03 and 0.045 W.m-1.K-1. There are two notable versions: expanded polystyrene and extruded polystyrene. - Polyurethane – is the best classical thermal insulator. Its thermal conductivity varies between 0.02 and 0.025 W.m-1.K-1. - Vacuum Insulated Panels (VIP) – a super-insulator in the form of vacuum panels.
This is the last stage in the logistics journey, culminating in the final destination. Health professionals and patients are an integral part of that last mile logistics.
“A document established by consensus and approved by a recognised organisation, that contains – for common and repeated use – regulations, directives or characteristics for activities (or their results) guaranteeing an optimal level of order in a given context” (a definition as set out by the ISO – International Organisation for Standardization – and the CEI). The norm is an indisputable standard on a given subject, suggesting technical and commercial solutions and used to simplify contractual relationships. To be considered as a norm, the document must fulfil two conditions: the means and the methods described must be reproducible, by using and conforming to the conditions indicated, and they must be recognised by all. In a general case the application of a norm is facultative but the law or regulations may render it obligatory. It may also be imposed by the principal to fulfil a contract.
Normalisation is the process by which norms are published and promoted. According to French regulations, the object of ‘normalisation’ is “to supply the reference documents containing solutions to technical and commercial problems concerning the products, goods and services that occur repeatedly within the relationships between economic, scientific, technical and social partners” (Decree n°84-74, 26/01/1984).
A patient-centric approach is one in which the patient is placed at the very heart of the health care system. It is based on a partnership between the patient, his family and the health professional to travel on an adapted treatment pathway together. Professional expertise and patient experience – acquired little by little throughout his life – are linked as both of them learn from the patient’s health and psycho-social problems, the illness itself and its implications on his lifestyle and that of his close family. This approach helps the patient to obtain self-caring skills, being able to adapt and manage his illness. through listening, monitoring and receiving support from the professionals throughout his treatment.
The phase-change materials (PCM) are materials that allow the storage of thermic energy by the solid or liquid sensitive phase and by the change in the solid/liquid phase. With fusion temperatures over or equal to 0 °C (positive), the PCMs allow the maintenance of the temperature differences between +2/+8 °C, +15/+25 °C as well as other specific temperature differences under specific hot or cold outdoor temperatures.
A temperature profile simulates the variations of temperature in a logistics circuit, from the moment the packaging is loaded until it is unpacked. The temperature profiles can be cyclic and composed of segments, or remain at a constant temperature. Some standards allow for pre-determined levels, others leave the choice and the responsibility to the user and the manufacturer.
The qualification relates to equipment such as cold chain packaging. It consists in showing, in a documented manner, the aptitude of the solution to meet the specific demands using norms or specifications. It confirms the performance of the solutions in pre-defined conditions through laboratory tests.
This is the optimum temperature to maximise and maintain healthiness and the security of the products inside an isotherm container.
This sensor contains a sensitive element to measure the temperature. A number of technologies involving temperature sensors exist. The most common are resistive probes (Pt 100 for example) and thermocouples.
This is a captor with a sensitive element which monitors temperature. Several temperature probe technologies can be seen working here; the most used are the resistive probes (such as Pt 100) and thermocouples.
Thermal stabilisation of a materiel is the maintenance of the temperature and its state at a predefined temperature.
Thermal stabilisation of a material is the conditioning of its temperature and its state at a predefined temperature.
This is a financial estimate covering the direct and indirect costs generated by the ownership and use of a product. For an isotherm packaging solution the calculation of the TCO will reveal the global financial impact of the solution. The purchase price is just one part of the global implementation cost, as transport, storage and preparation cost must be added – as well as conditioning and repatriation charges should the solution be reusable, After Sales Service is an additional expense to be considered, as are costs related to security risks such as loss, theft and temperature excursions.
This is a test carried out with an insulated or cooling packaging in a thermostatic case – this simulates the variations of the environmental temperature. It is then possible to qualify the thermal performance of the packaging by simulating various temperature changes in the surrounding environment. It is thus possible to qualify the case’s thermal performance and to check the capacity to maintain temperature-sensitive products within a required range of temperatures for a given period and a pre-defined temperature profile.
The validation relates to the complete transport procedure using the temperature-controlled packaging boxes. It consists in verifying and confirming in a documented way that the solution functions correctly in real-time conditions.
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