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Bluepharma
Bluepharma is a pharmaceutical company, of national capital, based in
Coimbra, Portugal. Basing itself on the excellence of the manufacturing
unit acquired from Bayer, one of the most advanced and well designed
in the country, and on the quality and training of its partners and the
experience and dynamism of its management team, Bluepharma is
one of the most dynamic and modern companies competing on the
Portuguese pharmaceutical market. Bluepharma was the first
pharmaceutical company in Portugal to operate with integrated
certification in accordance with ISO standards 9001 and 14001 and
OHSAS 18 001, and the first in the pharmaceutical industry to be
granted the EMAS environmental certificate, the most demanding
European environmental certification. The company has established
various partnerships for research and development projects that are
currently under way. With partners AIBILI and CNC, the company
entered a project for PRAI, and won the European Prize for Regional
Innovation for Portugal (2004) and recognition of project X-Prot. In
the industrial arena, and despite Bayer transferring all its production
to other countries, the company has managed to find enough clients and
projects to make use of the factory’s capacity, estimated at 10 million units
per year per shift. One of the biggest investment is taking place with the
aim of doubling the prodution capacity. In Portugal, the company has
developed its marketing of generic medicines reaching 30 medicines
on the market by December 2007. It has an office in Lisbon with 30
employees.
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Edol
Laboratório Edol, web site www.edol.pt is a pharmaceutical company
of exclusively Portuguese capital. It celebrated 54 years of age in 2006.
It has 86 employees, working in Administration & Finance,
Manufacturing, Quality Control, Regulatory Affairs, Medical,
Marketing and Sales, Research and Development and New Business
departments.
Laboratório Edol specialises in the development, production and
marketing of products in the following areas: Ophthalmology;
Dermatology, Dermocosmetics, Medical Devices. It also uses the excess
capacity of its production lines for contract manufacturing.
From 2001 to 2004, Laboratório Edol successively obtained, renewed
and integrated the following certificates; ISO 9001:2000 - Quality
(transition from ISO 9001:1995); ISO 14001 – Environment; OHSAS
18001 – Occupation Health and Safety and ISO 13 485 -Medical Devices.
Edol-Themaxis is a partnership with the Brazilian multinational,
Europharma. It is exclusively dedicated to the marketing of generic
medicines. It has a sales force of nine employees. |
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Grupo tecnimede
Tecnimede Group develops, registers, manufactures, promotes and
sells pharmaceutical products for human use.
The Group has three commercial companies (Tecnimede, Pentafarma
and Farmoz), one production unit (West Pharma), R&D facilities (Labor
Qualitas) and two foreign subsidiaries with commercial activities
(Tecnimede Morocco and Tecnimede Spain).
The production unit, West Pharma, is located in Lisbon. It specialises in
the manufacture of oral solid products and is accredited by IPAC and
certified in accordance with Good Manufacturing Practices (GMP) and
ISO 9001:2000.
Labor Qaulitas is located 40 km north of Lisbon. It is an R&D facility,
accredited by IPAC and certified in accordance with Good Laboratory
Practices (GLP) and ISO 17025:2005 and chapter 6 of GMP, which
allows it to conduct the batch release and certification of all types of
pharmaceuticals.
Through Labor Qualitas, the Group conducts research and development
of new chemicals, new forms of synthesis and pharmaceutical formulation,
analytical development and validation of processes, pharmacological
screening, toxicology studies, clinical studies.
Tecnimede Group has vast experience in conducting BD/BE studies,
working with CROs in Portugal, Spain, France and Canada, and has
developed a portfolio of more then 40 generic products at Labor
Qualitas. These are being registered in almost all countries of the
European Union.
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Laboratórios Azevedos
The history of AZEVEDOS covers more than two centuries. At present,
the structure has five areas of intervention (R&D, production, marketing
and sales, logistics and international). In the industrial area, SOFARIMEX
(Azevedos Group) is the leading Portuguese producer of medicines.
It specialises in small and medium batches, and exports more than
50% of its production. AZEVEDOS markets a wide range of products
ensuring a significant availability of prescription and non-prescription
products and hospital specialities. DLA Farmacêutica (Azevedos Group)
is responsible for the logistical operations of the Group’s companies as
well as of those of a significant number of clients. Since the beginning
of the 1990s, AZEVEDOS has pursued internationalisation as a strategic
target for its development. It exports to, licenses products or has direct
investments in more than 43 international markets. In terms of specific
direct investment, MEDIS is a key player in the Mozambique market.
LABORIS BRAZIL is the group’s second most important manufacturing
unit and serves the vast MERCOSUL market. A decisive step for the
evolution of AZEVEDOS was its commitment to R&D. As a result of
continuous research and a constant search for information with which
to exploit new opportunities, this area of intervention has opened up
new perspectives, the only way of enabling a constant improvement in
products and services bearing the AZEVEDOS brand. R&D has ensured
that AZEVEDOS is a leader in the sector and has focused activity on the
development of new pharmaceutical formulas, analytical methods and
productive processes.
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Luso Medicamenta
Lusomedicamenta S.A. is a pharmaceutical contract manufacturing
company operating in Portugal that specializes in the production of
solids, liquids and semi-solids.
We export about 58% of our production to 47 markets worldwide, and
we serve our clients, leading international pharmaceutical groups, with
the fullest range of and highest quality manufacturing solutions and
services. Facility design, together with fast changeover equipment, and
state-of-the-art information systems, optimises product and people
flow, providing very high flexible operations and reduced cycle times.
A dedicated and highly skilled technical team, and extensive
partnerships with national and international research and
development centres, provides our costumers with product development,
such as pre-formulation, formulation and analytical development, stability
studies, pilot batch production, and regulatory and technical support,
assuring full compliance during product life cycle.
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Medinfar
Medinfar is an independent and fully integrated Portuguese pharmaceutical
group with R&D, production, marketing, sales and distribution.
Besides its own products Medinfar markets licensed products in partnerships
with international pharmaceutical companies. The company
manufactures and markets prescription medicines in the following
areas: General Practice, Cardiology, Gastroenterology and Dermatology.
It also has activities in non-prescription products, clinical and
hospital equipment. Always maintaining its commitment to quality,
its well-trained workforce and state of the art manufacturing facilities
aim to bring products of the highest quality to worldwide markets.
Medinfar increased its productive capacity in 2001, with the acquisition
of an industrial unit, Farmalabor, in Condeixa. This unit has an area of
47,000 m2 of which 6,000 m2 are a covered area, this being the main
industrial unit of Medinfar Group. The design and construction of
Farmalabor facilities and equipments follow not only European Union
Good Manufacturing Practice (GMP) but also the cGMP UE. Farmalabor
is licensed to produce solid, semi-solid and liquid pharmaceuticals and
also cosmetics and body hygiene products. Our relationship with the
most important international companies, combined with a detailed
knowledge of the Portuguese market and a Guaranteed Quality product
system, has made Medinfar an important international partner, in
both Portugal and and new markets. Medinfar products can be found
in more than 20 countries all over the world.
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Tecnifar
Tecnifar is a family company, founded in 1969, and with 100%
Portuguese capital. Tecnifar is built on foundations of diligence,
dedication, training, flexibility, determination and courage. Tecnifar
markets its own non-patented products and products under licence
from research companies, for example, MSD, AstraZeneca, Roche,
Pharmacia, J. Uriach, Angelini, Sigma-Tau, UCB and HRA Pharma. The
Tecnifar Group’s portfolio is essentially made up of ethical medicines
in the therapeutic areas of neuropsychiatry, cardiology, gynaecology,
pneumology, dermatology, orthopaedics and others. Tecnifar is proud
to belong to the group of Portuguese companies that works with major
and credible international companies in close cooperation with medics
to contribute to a permanently evolving medicinal products market. Its
ethical but aggressive position in the market has allowed it to gradually
increase its income and the number of partnerships with recognised
research and development companies.
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