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    ADg Consultancy offers a range of services for the market access of pharmaceutical products and medical devices.
ADg Consultancy delivers service and support on both a long term and project basis, as well "on site" as remote.
For more details, please have a look to the website:

Agnes Degroote
Industrial Pharmacist
Gentsesteenweg 106
B-1730 Asse
Mobile : +32 479 98 92 88
Tel/fax : +32  2 452 34 68

    SMART&BI offers services in pharmaceutical market access (MA) including:
  • Price and Reimbursement
  • Compilation of the core value and reimbursement dossier
  • Feasibility analysis - value requirements
  • Relative Effectiveness, budget impact and HTA
  • Identifying the appropriate MA strategy
  • Stakeholder involvement
  • Monitoring of ongoing reimbursement procedures
  • Risk-sharing procedures and conditional reimbursement schemes
  • Competitive Intelligence and market analysis
  • Scope: BENELUX, France

Gebroeders Paters Abelooslaan 20
B - 1933 Zaventem
Tel +32 2 784 31 02

  INNOSENS = a team of 11 passionate professionals and a partner in the Netherlands at your service. 
Professional guidance and intellectual services in Market Access, Health Economics, Medical information
and Pricing and Reimbursement processes in the Benelux for drugs and medical devices, inluding adaption of BI and HE
models, development of GVDs, submisson and follow-up of P&R dossiers, MNPs/ETRs, networking/negotiations
with Health Authorities, KOL meetings/management, and strategic advice, as well as writing scientific articles/posters, and
last bu not least education and training. Our competitive prices and human-oriented approach is INNOvating with a big touch of SENSe.

Katrien De Groote (Founder/Owner)
+ 32 477 43 44 05


Based on > 30 years of experience, our main tools are a strategic approach, rapid service and clear communication on projects in the field of:

  • Regulatory Affairs: Regulatory submissions and life cycle maintenance including variations and renewals, GDP licenses, as well as post-approval activities, such as pharmacovigilance, promotional review
  • Market Access: Strategic advice, preparation of & support for pricing and reimbursement applications (BE/LUX)

Kathleen De Vrieze
+32 9 210 70 90 


We bring your medicines and healthcare products to the market and keep them there:

To achieve this mission, our multidisciplinary expert team offers hands-on support and advice in the following domains:

  • EU Regulatory Affairs
  • Market Access,
  • Pharmacovigilance,
  • Medical Information and Publicity,
  • Clinical Trials,
  • Quality Services,
  • Medical Writing.

For more information: 
+32 15 28 74 11 
Ludwig Everaert – general manager


INC Research is a leading global contract research organization (CRO) providing the full range of Phase I to
Phase IV clinical development services for the world's biopharmaceutical and medical device industry.

As a therapeutically focused CRO, with a Trusted Process® delivery methodology, developing the medicines
people need is something we take personally.
Leveraging the breadth of our service offerings and the depth of our therapeutic expertise across multiple patient
populations, INC Research connects customers, clinical research sites and patients to accelerate the delivery of new
medicines to market to improve world health. We were ranked "Top CRO to Work With" among large global
CROs by sites worldwide in the 2015 CenterWatch Global Investigative Site Relationship Survey.
INC Research is headquartered in Raleigh, NC, with operations across six continents and experience spanning more
than 100 countries

Our Vision
We aspire to be a leading innovator of clinical development services dedicated to providing differentiated
solutions to our customers

Our Mission Statement
We are an organization of therapeutically-focused high performance teams, led by world-class managers
and leaders, dedicated to helping our customers bring products to market to improve the health of
people around the world.

Our core values

  • Innovation
  • Trust
  • Leadership
  • Stewardship
  • Quality & Excellence
  • People

What we do
INC Research offers customers the following:

  • Strategic Clinical Development
  • Standalone Services
  • Pharmaceutical Consulting
  • Therapeutic Expertise

Leonardo Da Vincilaan 5, Caprese Building
1935 Zaventem


infarAMA bvba offers services for Regulatory Affairs, Quality, Vigilance, Information & Publicity
and Translations from small local to world-wide leading health care companies for medicinal products,
medical devices and food supplements.

Our mission is to take care of your technical, scientific and administrative projects when you are
in need of a partnership with an experienced team. Our know-how, based on more than twenty
years of experience, guarantees an accurate realisation of your projects.

It’s a pleasure working together!

Noëlla Heyman and Marian Coquel (co-founders)
+32 11 31 26 16 –
For more details, please visit our website


KDT is an independent consultancy bureau providing support and advice in regulatory affairs,
pricing and reimbursement, distribution & storage, information & publicity and pharmacovigilance
of medicinal products for human use within Benelux.

We are in a position to provide high standard professional regulatory expertise covering

  • development,
  • submission and
  • post marketing requirements

of medicinal products for human use.

Consultancy of different kinds can be provided on a remote basis from our office or on site at your premises
if this is more appropriate. A combination of both can be agreed upon.

Contact details

KDT - Hemelrijk 9, B-9402 Meerbeke

Phone: +32 54 32 09 23


As a full service CRO with two decades of experience directing Phase I – IV clinical development
programs leading to more than 230 product approvals, SynteractHCR has proven it is uniquely
positioned to help clients successfully navigate the complex drug development process.

Yves Ampe
Managing Director
SynteractHCR Benelux n.v.
Keizer Karellaan 576
1082 Brussels
Tel.: +32 2 4643966


AML Clinical Services is a CRO (contract research organization) that provides focused
clinical research services to pharmaceutical, medical device and biotechnology companies,
CROs and research sites.

A dedicated team of qualified research professionals is available to assist in any stage of the
conduct of  clinical trials, in any therapeutic area.  We have experience in pre-marketing as
well as late phase and post-marketing trials.

It is our mission to make each and every clinical trial a success by reducing study start-up time,
meeting project timelines and assuring high quality clinical data.

With our CAN DO attitude we turn problems into challenges to manage.  And while doing this, we
value team work as well as integrity, open communication and mutual respect.

AML retains a small-scaled organization to guarantee close oversight, commitment,
loyalty and low turnover. Our employees are valued for their high experience, knowledge,
flexibility and dedication to their responsibilities.

Contact details:

Anne-Mie Lenaers
Tempelzicht 8, 3210 Linden, Belgium
Phone: +32 16 78 21 70


MedDb services

Database related web applications
Intranet and extranet applications
Web based DMS (Document management system)
Web technology integrated with powerfull CMS and CSS
Consult - project management web and db technology
Data analyses in BO (Business Object)
E-mail marketing platform
Online agenda management


Keizerplein 42
9300 Aalst
Phone: +32 (0) 53 21 08 48


Pharm-Olam International is a multi-national Contract Research Organization (CRO)
offering a wide range of comprehensive, clinical research services to the
pharmaceutical, biotechnology and medical device industries. From Phase I to
Phase IV, Pharm-Olam focuses on delivering the highest quality data, achieving
targeted enrollment and meeting projected timelines. For further information about
Pharm-Olam, please visit

Pharm-Olam International (Belgium) BVBA
Dorp 14a
3272 Testelt


IQVIA (NYSE:IQV) is a leading global provider of information, innovative
technology solutions and contract research services dedicated to using analytics
and science to help healthcare stakeholders find better solutions for their
patients. Solutions are powered by the IQVIA CORE TM, which combines big data,
advanced technology, analytics and extensive industry knowledge. Formed through
the merger of Quintiles and IMS Health, IQVIA has approximately 55000
employees worldwide. Learn more at

Davos Builing Da Vincilaan 7
1930 Zaventem

IQVIA Integrated Engagement Services
Medialaan 32/2
1800 Vilvoorde

Reception T: + 32 2 627 32 11 (Zaventem) - Reception T: + 32 2 555 05 55 (Vilvoorde)
Ms Tamara Denie - Marketing Manager
T + 32 2 627 32 15

M + 32 496 25 15 39


Covance, a unit of LabCorp since Feb. 2015, with headquarters in Princeton, New Jersey, is one
of the world's largest and most comprehensive drug development services companies,
employing approximately 12,000 employees worldwide in more than 60 countries.

Working with the world's top 50 pharma and biotech companies, Covance is extremely proud to
have touched 1/3 of all drugs on the market today.

Our project teams are passionate about delivering excellent customer service and unfaltering science.
Our whole team takes pride in and has passion for what we do. As an integral part of this team,
our employees make a difference in the lives of millions.


Covance Clinical and Periapproval Services SA
Avenue Marcel Thiry 77, 1200 Brussels, Belgium
T +32 2 773 2911| F +32 2 772 2998


Van Bael & Bellis - Firm description

Van Bael & Bellis is a leading independent law firm based in Brussels. With nearly 70 lawyers coming
from 20 different countries, we offer our clients the support of a highly effective team of professionals
with multijurisdictional reach and an international perspective. Our expertise is focused and
specific, resulting in deep experience within our specialisations of EU and national competition law,
EU trade and customs law, regulatory law as well as Belgian business law.

Van Bael & Bellis is a leading life sciences firm offering specialised advice to innovative
pharmaceutical, biotechnology and medical devices firms.

Van Bael & Bellis – Contact details

Peter L’Ecluse – 02 7904 934 –
Catherine Longeval – 02 7904 950 –


IN2Pharma offers support and guidance in regulatory affairs, quality assurance, medical affairs
like medical writing, information & publicity and pharmacovigilance and has unique experience in the
set-up and conduct of post-marketing (clinical) studies.

Our team of 9 ensures a professional and confidential conduct, a dynamic approach and an accurate
and fast follow-up of your project. Our consultants are experienced, dedicated and flexible and can
operate from the IN2Pharma offices or on site in your offices.

Caroline Steensels
IN2Pharma NV
Terloonststraat 22
1910 Kampenhout 
T +32 16 89 16 00  

  Deloitte is a leading professional services firm with a prominent Life Sciences industry practice. 

We support our clients across the value chain (R&D, Supply Chain & Operations, and Commercial) as
well as with more strategic services such as mergers & acquisitions, and enabling services such as tax
and accounting. Deloitte has more than 3.000 employees in Belgium with Life Sciences being our
largest Business Sector. Please visit us at


Voor strategische vragen of opmerkingen rond het partnership:

Tom Van Wesemael
Gateway building
Luchthaven Nationaal 1J
1930 Zaventem
+ 32 2 749 58 12

Management Assistent Tom Van Wesemael:
Veerle Debergh
+ 32 2 749 59 86


The PwC global pharmaceuticals and life sciences practice is made up of over 2,800 dedicated
specialists in the pharmaceutical and life sciences industry. Working closely with our clients,
ranging from small entrepreneurial life science companies to large global corporations, we aim
to achieve increased performance by improving the efficiency and effectiveness of a company’s key
business operations.
Across the whole Pharmaceutical and Life Sciences value chain, PwC’s trusted consultants and
professional advisors use their wealth of industry based experience, knowledge and expertise to
help our clients evaluate their strategic business options, improve management and control, and
identify cost saving initiatives.
At a local level, PwC Belgium has created a special cross-services “pharma team” to better
serve the industry’s needs. This team comprises more than 60 professionals from various
departments (Audit & Assurance, Tax & Legal Services, Advisory Consulting) dedicated to
supporting pharmaceutical & life sciences companies in addressing the issues and challenges specific
to the sector. Being part of a global network gives the Belgian team access to a pool of specific
expertise from around the world, enabling us to address the challenges of multinational pharmaceutical
& life sciences organisations.

PwC Contact details

Didier Delanoye
Woluwedal 18
B-1932 Sint-Stevens-Woluwe  
+32 2 710 4104


PPD is a leading global contract research organization providing comprehensive, integrated
drug development, laboratory and lifecycle management services. Our clients include
pharmaceutical, biotechnology, medical device, academic and government organizations. With offices
in 46 countries and more than 16,000 professionals worldwide, PPD applies innovative
technologies, therapeutic expertise and a firm commitment to quality to help clients deliver
life-changing therapies that improve health.

Contact details:

Hilde Dhont
Sr. Country Manager, Site Intelligence and Activation
Kleine Kloosterstraat 23
1932 St. Stevens Woluwe
Phone +32 (0) 2 723 28 34
Cell +32 (0) 479 95 97 03


MEDIMIND SA/NV offer 3 types of services:

1/ Improvement of therapeutic adherence:

With his innovation the « Posomind », the first dedicated device that helps the patient to take his
medication correctly, Medimind is specialized in the improvement of therapeutic adherence.
We support pharmaceutical companies in Clinical Studies, Survey, PSP & Market Access.

2/ Data Management: 

We generate data analyzes related to the behavior of the patient thanks to the data resulting from
the use of Posomind.

 3/ IT support: 

We are Specialized in IT Development – Testing – Technical Analysis – Integration and Project
Management. More than 70 IT specialists serving the needs of the pharmaceutical industry.


Bernard Hiernaux
M +32 477 45 46 81
Sentier du Berger 43
1325 Corroy-Le-Grand 


XPE Pharma & Science is a full service organization specialized in HR & Project Services in the life sciences

We are a leader in Talent Solutions for pharma, biotech, medical devices, diagnostics, R&D and consumer

Our 4 domains of expertise are Clinical, Technical, Medical and Sales & Marketing.

We also have a dedicated team specialized in Medical Writing, Publication & Document Management,
Patient Support Programs & Real World Evidence.

CMAST provides consultancy, project management and tangible business solutions to pharma & life
sciences companies, universities & research institutes.

We are active in the following domains: 

• Early Stage Innovation • Grant Management & Public Funding • Project & Portfolio Management
• R&D Process Optimization • Multi-stakeholder Collaborations • Regulatory Compliance & Quality
• Health Data Analytics & Visualization • Supply chain.

With a team of more than 90 industry experts, we are passionate about assisting our clients in the
creation and development of innovative healthcare solutions.

CMAST and XPE Pharma & Science are both part of the Modis Group, and are working together closely
– which allows us to connect life sciences businesses and talent in a fast-changing world!


e&a is your partner in health policy consultancy, offering services in Strategic Advice, Market Access,
Public & Regulatory Affairs. It is our objective to help developing your business and the many disciplines
of your company, resulting in an increased efficiency and business result.

Our main domains of expertise are:

  • Strategic advice for company, portfolio and product resulting in Operational plans
  • Market Access: Defining strategy, preparing the application, negotiations for achieving results
  • Public Affairs: Stakeholder mapping and engagement processes
  • Regulatory Affairs activities for medicines, medical devices and food supplements


e&a, health policy consultants
Lindenberg 16
B-3080 Vossem
+32 (0)477 29 34 04


Diapharm is een internationaal toonaangevend dienstverlener en adviesorganisatie voor humaan- en
veterinair geneesmiddelen, medische hulpmiddelen, voedingssupplementen en cosmetica; met
vestigingen in Nederland, Duitsland, Oostenrijk en China.

De firma biedt aan ondernemingen succesvolle ondersteuning op het gebied van R&D, Regulatory
Affairs, vergunningverlening, medisch-wetenschappelijke vraagstukken, kwaliteitsborging,
farmacovigilantie, analytische testen en productie van gezondheidsproducten. Diapharm ontwikkelt
vooral OTC productinnovaties.

De firma begeleid klanten met Registratie /conformiteitsbeoordeling, marktintroductie en
dossieronderhoud van medische hulpmiddelen en IVD.


Dr AH Verhage (CEO)
Diapharm  B.V. 
Graaf Engelbertlaan 75 (Bondpark)
4837 DS Breda, Nederland


CMS Belgium and its 100 lawyers in Brussels, Antwerp, and Luxembourg provide complete legal services.
We offer an in-depth expertise in life-sciences related matters to private companies and public actors,
at a local level as well as internationally. We cover a.o clinical trials, regulatory, public procurement,
data protection, e-health and human samples.
We set up multidisciplinary ad-hoc teams whenever the matter requests it.
Discover our other practices by surfing on

CMS Belgium belongs to CMS, founded in 1999. CMS is the leading European legal services provider.
More than 4,500 legal professionals in 70 offices and 39 countries are ready to serve you whenever
you need it.


Bruno Fonteyn
Senior Associate
T +32 2 743 69 86
M +32 476 45 25 85
F +32 2 743 69 01

CMS Belgium, Chaussée de La Hulpe 178 1170 Brussels


HOYNG ROKH MONEGIER is a law firm located in 5 European countries, specialized in all areas
of intellectual property and pharmaceutical regulatory services.

What sets us apart is a very strong and experienced patent practice, with expertise in leading
blockbuster pharmaceutical patent cases and in pioneering biotech cases and medical device
litigation proceedings, combined with a top notch pharmaceutical regulatory practice.

More than 50 members active in the pharmaceutical industry, animal healthcare as
well as manufacturers and distributors of food supplements have regularly relied on our lawyers’
services the past 5 years.

Liesbeth Weynants
Nervierslaan 9-31 Avenue des Nerviëns, 1040 Brussels
T 02 740 00 63


Allen & Overy is an international law firm with offices in Brussels and Antwerp, and has been in
Belgium for over 30 years. Our dedicated Life Sciences team acts on a broad range of strategic
matters on a daily basis. Our expertise includes high-profile patent litigation, licence agreements,
parallel import issues, pricing and reimbursement issues, clinical trials, IPOs, acquisitions, merger
control, state aid advice and employment law. We act for a broad range of companies, from start-ups
and spin-offs to major pharmaceutical and biotech companies. Our unique experience of
working with innovative companies has enhanced our ability to identify the latest trends in the life
sciences sector.


Allen & Overy (Belgium) LLP
Tervurenlaan 268A
1150 Brussel
T:+32 2 780 2222


Remedus offers services to optimize health outcomes for patients, through supportive nursing,
mobile health and logistic solutions, focusing on improving medication adherence and quality of life.

These outcomes need to be measurable, both for the benefit of users and to demonstrate the value
of the program and the associated drug to HCPs, payers and providers.

Our main domains of expertise are:

  1. Patient Support Programs
  2. Risk Minimization Programs
  3. MNP / ETA Programs

Remedus is a market leader in designing, developing and delivering programs for specialized homecare,
mobile health (telemonitoring), and patient coaching/education.

Remedus is ISO13485 certified.


Boomsesteenweg 44
2630 Aartselaar
+32 3 870 43 90 


Eurocept Homecare is één van de grootste aanbieders van medisch specialistische thuisbehandelingen
in Nederland. We combineren een farmaceutische groothandel, een openbare apotheek, een landelijk
netwerk van verpleegkundigen en een op patiënten toegespitste logistieke service. We leveren naast
medisch specialistische geneesmiddelen, ook medische hulpmiddelen. Onze diensten worden uitgevoerd
in opdracht van medisch specialisten, ziekenhuizen, diëtisten, verpleegkundigen, patiënten, zorgverzekeraars
en farmaceutische bedrijven. Wij streven ernaar om het dagelijks leven van patiënten zo min mogelijk
te verstoren. Zijn wie u bent ongeacht de aandoening en/of medische (hulp)middelen die u (nodig) heeft.
De diensten van Eurocept Homecare zijn beschikbaar in heel Nederland en over de grens in België
en Duitsland.

Eurocept Homecare
Loodsboot 7
3991 CJ Houten
+31 (0)30 - 280 42 71 
Buiten reguliere openingstijden is er een nooddienst 24/7 bereikbaar via +31 (0)30 - 280 42 71


Qplus Consult offers specialised services for the (bio) pharmaceutical industry.

Production plants, distributors and warehouses in Belgium and abroad can rely on Qplus Consult's
many years of experience in Quality AssuranceRegulatory Affairs, Pharmacovigilance & medical
affairs, GxP/ISO audits and training. Our team of enthusiastic, high-level consultants, who are
dedicated to providing optimum service, is hard at work every day. 

Implementing, maintaining or integrating quality systems, the release of medicines for the European
or local market, quality control of artwork and all packaging materials, internal and external audits,
drawing up CAPA plans, etc. are just a small sample of the wide range of services Qplus Consult
can offer. Implementing an efficient communications flow and reporting as well as regular consultations
with clients form the foundation of our successful collaboration. Thanks to extensive internal and
external training, Qplus Consult's consultants remain up to date and work according to the most
current legislation and regulations.

Those who choose Qplus Consult know that information is treated with the utmost confidentiality and
in the safest possible manner. Those who choose Qplus Consult know that our work is carried out correctly
and efficiently, ensuring that our services provide your company or organisation with more than just
added value.

Qplus consult BVBA
Leuvensesteenweg 643 bus 7
1930 Zaventem
Tel: 0032 2 899 05 68


COMPASS Pharma, founded in 2018 by Sandy Sercu and Melissa Penninck with both having already
a lot of experience in medical writing, delivering strategic advice for price and reimbursement of
medicinal products and medical devices, set-up of non-interventional studies and medical need
programs, is focused on:

  • Price and reimbursement applications in Belgium and Luxembourg
  • High level strategic advice in entering the Belgian market
  • Set-up of non-interventional studies to collect real-world evidence
  • Medical need programs
  • Compassionate use

COMPASS Pharma is located in Sint-Katelijne-Waver with a second branch in Lebbeke.

COMPASS Pharma can be contacted by

  • Email:
  • Phone:
    • Sandy Sercu (+32 485 62 89 46)
    • Melissa Penninck (+32 477 65 80 57)

PSI is a privately-owned, full-service clinical research organization (CRO) operating globally.
PSI’s global reach supports clinical trials across multiple countries and continents, and is known to
be highly selective about the work that they pursue. With an exceptionally high repeat and referral
business rate combined with minimal staff turnover, PSI is committed to being the best CRO in the
world as measured by its customers and its employees.


Brusselsesteenweg 66
3000 Leuven
+32 16 14 01 71


IM Associates, strategic partner of pharmaceutical companies

We help you optimize your market insights and your commercial approach towards prescribers and
hospitals. Besides that, we gladly share with you our knowledge of the pharmacist's role and the elderly
houses segment.

Areas of expertise:

  • Go-to-market models (incl. multi-channel);
  • Patient flow analytics & budget impact studies;
  • Key Account & Tender Management (hospitals, pharmacy groups & elderly houses);
  • Analytics: IM Smart is our mobile platform for the monitoring of your sales and customer interaction.

Let’s get in touch!

Jurgen De Baerdemaeker, CEO
Tel +32 16 22 47 43

IM Associates
Persilstraat 52/E – bus 5
3020 Herent


PhaRA is a consultancy firm in BENELUX and EU Regulatory Affairs providing strategic and hands-on
support to Pharma & Biotech companies.

By focusing exclusively on regulatory affairs, PhaRA can offer in-depth expertise and skills covering a
broad range of RA activities for chemical entities and biologicals.

Our BENELUX services and expertise cover submission and maintenance at national level of MAA for Rx
and OTC products, notifications for borderline products, compassionate use and medical need programs,
support to RMA and DHCP letters. PhaRA is the selected provider of the Clarivate BELUX regulatory
intelligence services.

Our EU services cover all activities during development and life cycle management, including:

  • scientific advice, paediatric investigation plans (PIP), orphan drug applications
  • regulatory scientific writing
  • labeling development and remediation
  • strategic advice in early and late phase drug development
  • clinical trial and marketing authorization application (CTA/MAA) preparation and MAA filing
  • running EU procedures (CP/DCP/MRP)
  • liaising and meetings with EMA, FAMHP and other national competent authorities
  • life cycle management
  • regulatory due diligence activities
  • regulatory affairs intelligence services and training

Therapeutic areas of special interest include early phase development, infectious diseases, immune
inflammatory diseases, (immuno)oncology, vaccines, and other unmet medical need areas.



Roosevelt Building
Anneessensstraat 3-5 B9
T +32 3 293 90 84 and


Hygeia Projects BVBA offers services in pharmaceutical market access


Nancy Dams
Managing Director
Hygeia Projects BVBA
Da Vincilaan 1
1930 Zaventem
0496 58 51 35


HCC has the ambition to a strategic partner for Pharma and Biotech companies in delivering
valuable Strategic Support for your Market Access Challenges.  We will guide your 
Innovative Health Technology to the Market by performing innovative Market Access activities
tailored to your specific needs.  HCC has the knowledge of the Belgian Payer Dynamics in
different therapeutic domains and specific Market Access Disciplines, making us a Valuable
 for different kind of projects. With our industry leading expertise we guarantee you to
successfully overcome every Market Access hurdle at any stage of your product or company lifecycle.


For more information please visit our Website:

HCC bvba
Sven Tops – CEO 
Velm 18
1730 Mollem


Realidad, a small company specialised in real-life data analysis for decision making, combines
many years of clinical and economic expertise to provide tailor-made solutions for all your real-life
data needs.

  • Services include:
    • Patient chart reviews: retrospective and prospective
    • Patient registries
    • Expert panels
    • Expert Interviews
    • Unit cost collections
  • Domains of expertise include:
    • Oncology/Haematology
    • Dermatology
    • Gastro-enterology
    • Cardiology
    • Vaccines
    • Neurology
    • Etc.

Contact: Daniëlle Strens,
owner Realidad bvba
Address: Wezelstraat 56, 1850 Grimbergen
Tel: +32(0)478566004


HVO Consulting is a dedicated partner for pharmaceutical companies with expertise in:

  • Market Access
    • Price and reimbursement dossier compilation, strategy and support
    • Price management
    • Managed Entree Agreements: reports, advice and support
    • Training
  • Medical Information and Publicity
    • Promotional review
    • Training


HVO Consulting BVBA
Helena Van Overloop
+32 485 32 58 12


SGS is a CRO providing clinical research and bioanalytical testing with a specific focus on early
stage development and biometrics. Delivering solutions in Europe and in Americas, SGS offers
clinical trial (Phase I to IV) services encompassing early phase drug development consultancy,
clinical monitoring, biometrics and regulatory & medical affairs services. SGS has its own clinical
unit in Belgium including a Human challenge testing facility and two phase I patients units based in
Belgium and Hungary.

SGS has a wealth of expertise in FIH studies, viral challenge testing, and complex PK/PD studies
with a high therapeutic focus in Infectious Diseases, Vaccines, and Respiratory.

SGS Belgium
Generaal De Wittelaan 19 A Bus 5
2800 Mechelen
+32 15 27 32 45


SILLAR CLINICAL is a CTMO, a Clinical Trial Management Organization, providing solutions for our
customers ranging from the design, over the set-up, to the full management of clinical trials. We
primarily focus on phase I, II  and IV clinical trials, within Europe. Our customers are biotech,
pharmaceutical companies and academic researchers. Our headquarters are located in Ghent, the
biotech capital of Europe.

Running clinical trials is highly regulated, unique and truly complex. Our adaptive approach
and clinical trial expertise complements the inhouse scientific knowledge of the customer.
We guarantee regulatory compliance and customized conduct of clinical trials within time and budget.

Xavier de Cocklaan 66 / 3
9831 Sint-Martens-Latem
Tel: +32 9 395 23 60



Studio Pharma, a team of regulatory affairs professionals willing to go the extra mile to satisfy your needs for high quality services, on time and within budget.

Experienced in RA, QA and PV - for local and global companies - medicinal products, medical devices and food supplements.

Isabelle Geeraert
Tel: +32 496 85 87 49




With over 240 experts globally and a wealth of hands-on experience from working inside life sciences companies and regulatory bodies, clients choose us as their strategic partner to guide them through some of their most complex legal challenges.

Marc Martens
Bird & Bird (Belgium) LLP
Louizalaan 235
1050 Brussel