Articles
30.05.2018
We’re hiring! Are you the Sales Coordinator we are looking for?
Taipuva consulting is looking for a self organizing and diligent Sales Coordinator to our office in Tampere. Position requires fluent Finnish language skills, so the rest will be in Finnish. Sales Coordinator, Taipuva Consulting Oy Taipuva Consulting Oy etsii yhdessä...
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Articles
30.04.2018
Taipuva is Smart Expert Polarion
Taipuva is now Smart Expert – Polarion Last week Taipuva Consulting Oy received a recognition by Siemens PLM Software as a Smart Expert Polarion. "This confirms the expertise of Taipuva in this area", says Tony Jolly, Vice President Channels EMEA,...
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Events
19.02.2018
Taipuva ALM Solution Day 2018
Taipuva ALM Solution Day 2018 was a great success! We hosted close to 100 hundred participants from about 30 different organizations and heard excellent speakers from Fortum Innokas Medical NIRA Dynamics KTH Royal Institute of Technology Siemens PLM Software Ideal...
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Articles
09.02.2018
Requirements Engineering Glossary available for download
Our glossary offers a good starting point for defining requirements engineering related terminology at your company. Just download the simple Excel format glossary and modify it to suit your company's needs! Requirements engineering (RE) is a field with many terms and...
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Articles
05.02.2018
Taipuva is Top Siemens PLM Partner Nordic
We just finished our first Siemens PLM fiscal year, and what a year it was - we were the Top Partner in the Nordic region 2017! We were excited to receive the award at Siemens PLM Software's European Partner Leadership...
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Articles
07.12.2017
Upgrade from DOORS to a new all-in-one solution!
The good old Rational DOORS has served well, but it's... Well, getting old. The Next Generation DOORS (NG) is a completely different platform. It means that one thing is inevitable: change. A change is also a possibility. Take control...
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Articles
06.12.2017
How to ease medical device development?
In this article I address four (4) different aspects for you to consider, when aiming to improve your ways of working. The context is medical device product development (incl. software) and the regulatory requirements of the industry – meaning the...
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Articles
23.11.2017
Medical devices, boost your way into Polarion ALM!
Where to start when there are so many things to consider? Compliance to standards and regulations (e.g. IEC 60601, Medical Device Directive 93/42/EEC and FDA CFR 21 parts 11 and 820), safety risk management (e.g. ISO 14971), approval processes...
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