Categorized as: Process Management

We are moving to new offices in Ørestaden

1st of October 2014, we’ll be moving to our new modern office space in Ørestaden with plenty of room for both development and growth.

We have in recent years experienced a significant increase in demand and positive growth within our competences: End-to-End Medical Device Consulting, Research & Development, Quality Assurance and Regulatory Affairs.

We have a clear ambition for further growth and a desire to expand our network of customers and partners. With the new office we will have plenty of room for both development and growth.

We look forward to move into our new office, which is located in an international environment in Ørestaden and centrally located for the metropolitan area, Southern Sweden, train, metro, the highway network and Copenhagen airport.

IMG_3686

Our new address is:

Medicologic A/S
Arne Jacobsens Alle 15-17
2300 København S

You can still contact us using the same telephone numbers and emails.

We look forward to inviting you to our new office.

Best regards,
Medicologic

Continuous training is keeping us a step ahead

Medicologic is an innovative company believing that expertise builds confidence with the customers. In order to develop our expertise and add value to the projects we manage, we believe that continuous training is a must.

Recently all Medicologic employees took part in a tailored training program on business-oriented project management and agile project management. Methods that we feel certain are key to well-driven and successful projects.

Training

The program provided our team with powerful and innovative frameworks and tools to help customers bring their products to the market successfully. Tools that strengthen our consultants in keeping the right balance of time, product features and resources needed at any given time of the project. Through agile project management we can secure a high quality end product by keeping track of milestones and always match the expectations of our clients.

At Medicologic we have experienced that continuous training and streamlining of our tools and processes brings us a step ahead and we feel confident that we will continuously add value to our customers’ projects by using the know-how derived from ongoing training in our daily work with our customers.

Contact
Martin Thomsen
Teamleder, Product Development
mt@medicologic.com
Phone: +45 22 47 72 12

Creating value for our customers

“Medicologic is an innovative company that knows how to balance customers’ demands, in terms of high quality and just in time requests”.

So declares Lone Jager Lundquist, CEO at CarouCELL, who is very pleased with the cooperation with Medicologic.

These words make us very proud as we believe that our understanding of the customers’ needs and wants, the ability to keep costs down and our on-time delivery of end-to-end consulting services are creating significant value for our customers.

Team-Medicologic

Furthermore we were earlier this year chosen as the only Scandinavian company by the Japanese Nomura Research Institute (NRI) to take part in a European research. We believe their choice validates the fact that global companies as well can trust in our expertise, ability and capability of delivering a high level problem-solving process.

Through our services we feel sure we are meeting market demands which is also documented in our financial report as we managed to grow our business with a revenue growth of 50,3 % in 2013.

We believe we are now ready to set our sights even higher for both our customers and Medicologic in the future and we are looking forward to serving you after some well-deserved holidays.

Best wishes of a fantastic summer from the Medicologic Team!

Are you ready for the new UDI legislation?

FDA has approved UDI legislation – Europe is on its way
As part of the steadily increasing requirements for medical devices, the FDA has approved a new law that provides specific requirements for a unique marking of medical devices – UDI, which stands for Unique Device Identification.
The new system will ensure that reporting of serious incidents are more precise, while making it easier for authorities and users to gather and analyze data from the market.

What does it mean to your business?
The legislation will enter into force on 24 September 2014 and will apply to all medical devices sold in the United States. A similar requirement is expected to be adopted in Europe. To many manufacturers of medical equipment it means modified workflows, new needs for data handling and increased costs.

When will the legislation be relevant to you?

UDI-timeline-1

Getting Started
Medicologic, in collaboration with the American software house PTC offers coaching and counseling as well as an out-of-the box software solution for handling of the new requirements. Our specialist consultants will help in the process from needs analysis to implementation and training.

Want to know more?
Asger Dahlgaard
Program Manager, B.Sc Engineering

Direct (+45) 22 47 41 06
ad@medicologic.com