Within a few weeks the TIM User Group Meeting will take place. Official Registration is open and a lot of people have already pre-booked their attendance.
To assure you are able to attend, please register asap by email: usergroupmeeting-TIM@triskelion.nl
We will share updates on the technology, methodology and recent applications of the TIM systems in pharma and food.
The program will be shared soon.
Costs for attendance are € 375,- (excl VAT).
Online edition is to be found below…. In Dutch.
Its about “New Innovative Medicines needs new innovative testing methods.” We are more than happy to go through it with you.
Following our previous announcement on Triskelion’s altered services portfolio, we would like to give you an update on the latest development.
We are pleased to inform you that Triskelion has decided to continue the performance of (bio)analytical studies under GLP. As such we are still able to ensure and deliver services with the highest applicable standards (GLP and ISO 17025 quality and expertise).
We are looking forward to present to you our new strategy by the end of 2018.
At this moment we continue to deliver best in class solutions in the area of:
- Nutrient analyses
- Genetically modified Organisms (GMO) analyses
- Authenticity analyses
- Emergency Response Service (ERS)
- Registration Services & Risk Assessment
- Packaging (migration, petitioning and compliance)
- TIM: gastrointestinal models (services & lease)
- (Bio) analytical services (GLP and non-GLP): method development, validation and sample analyses
We are happy to discuss your current and future needs.
Might you have any queries or questions, please feel free to contact us: email@example.com.
We would like to ask your attention for our upcoming TIM lab days. During these days, we will showcase the newest TIM technology additions like the new stomach compartment and new TIM table top model at our facilities in Zeist, The Netherlands. During these TIM lab days you will get a deeper understanding of the use and capabilities of our TIM technology. To see more of our TIM models, please click here.
We would very much like to learn if this is of any interest to you. If so, would you please be so kind to let us know your availability during the last quarter of 2018 or spring of 2019?
Please send an email with the dates of your preference to firstname.lastname@example.org with the following subject note: ‘availability TIM lab days’.
We look forward to receiving your positive feedback and welcoming you to our TIM lab days.
If you would like to receive additional information, pelase do not hesitate to contact us via e-mail or phone +31 (0)6 5280 3578.
We proudly announce that the Registration Services & Risk Assessment team of Triskelion enabled all of their REACH clients to comply with the 3 major legal deadlines in 2010, 2013 and 2018.
Years of helping clients with their registration strategies, data gap analyses, SIEF discussions, pushing for early action, outsourcing and monitoring studies, creating IUCLID files, preparing read-across justifications and exposure assessments paid off as we were able to send the final files and dossiers to the clients well before the final deadline of 31 May 2018.
By focusing on being proactive, applying strong project management techniques and putting our experience collected through years of service into practice, unpleasant surprises were kept to a minimum.
For substances with ongoing studies we ensured eligibility for the Directors Contact Group solutions. Our structured approaches and familiarity with relevant tools ensured that we could finalize quality dossiers in time.
All in all, thanks to good preparation and experience we were able to make our clients happy, delivering a few hundred high-quality REACH dossiers ranging from relatively simple dossiers to very large dossiers with lots of data or extensive use of read-across and other alternative approaches. Simultaneously with these activities, we were also meeting the needs of our clients in the scope of the Biocidal Products Regulation.
And, of course, the REACH-related activities continue: dossiers have to be updated and resubmitted, the communication with ECHA on (draft) decisions and approval of test proposals continues, downstream user communication is getting more attention and clients need support in the scope of restriction or authorization processes.
We look back on fruitful and successful cooperation with our clients before the REACH deadline and we look forward to continuing our support for the chemical industry with our regulatory services in the future.