QbD Group Email Formats

Business Consulting and Services • Antwerp, Flemish Region, Belgium • 501-1000 Employees

QbD Group Email Formats

QbD Group uses 5 email formats. The most common is {first initial}.{last name} (e.g., j.doe@qbdgroup.com), used 47.1% of the time.

Format	Example	Percentage
{first initial}.{last name}	j.doe@qbdgroup.com	47.1%
{first name}.{last name}	john.doe@qbdgroup.com	37.1%
{first initial}.{second initial}{last name}	j.odoe@qbdgroup.com	5.7%
{first initial}{last name}	jdoe@qbdgroup.com	3.8%
{first initial}.{second initial}	j.o@qbdgroup.com	3.3%

Key Contacts at QbD Group

Jose Decolsa

Sales Director Qbd Group Spain

Peter Goossens

Marketing Director

Wim Steenackers

Sales Director International

Dmitry Obolskiy

Associate Director Regulatory Affairs

Baiyang Li

Business Development Director China

Pilar Rotaeche Montalvo

Director

Company overview

Headquarters	Groenenborgerlaan 16, Antwerp, Flemish Region 2610, BE
Phone number	+3238444501
Website	qbdgroup.com
NAICS	5416
Keywords	Regulatory, Auditing, Medical Devices, GMP, Consultancy, QMS, Validation, Biotech, Quality Management, Qualification, MDD, GLP, Gdp), Technology Transfer, GDP, Serialization, QbD, MDR, Data Integrity, Gamp5, Training (Gmp
Employees	501-1000
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About QbD Group

The QbD Group supports life science companies worldwide throughout the entire product lifecycle – from idea to patient. We are a global company with over 700 high-qualified employees. Our experienced team serves the wider life science industry, with a strong focus on ATMPs, medical devices, IVDs, and digital health, thanks to the specific expertise we have built in these areas. The services we offer fall under the following divisions: • Regulatory Affairs: We help our clients in their journey throughout the entire drug and medical device regulatory lifecycle. • Clinical: We are an expert clinical solutions provider specialized in medical devices and biotech, offering global CRO services and consultancy. • Qualification and Validation: We guarantee that products meet quality demands and comply with regulation through the qualification and validation of your processes, equipment, and software. • Quality Assurance: We offer the full range of QA services necessary to get your product to market in a safe and compliant way, including auditing from certified auditors, setting up your QMS, and all QP (Qualified Person) activities. • Quality Control: Our QC division consists of a GMP laboratory that offers analytical services for testing pharmaceutical raw materials, excipients, and release testing of finished products. • Software solutions: Cloud-based and pre-validated Quality Management Software built for the life sciences, as well as eIFU services which enable IVD and MD manufacturers to digitalize paper Instructions For Use (IFU). • Go to market: We help you launch your product to market by providing marketing and communication services, business development support and sales strategy.