The CRO with strong data management and statistical background
A good study design is the key of success
Reliable results can only be produced from perfect data.
The scientific results can only be answered with the help of statistics
Process management and more
Planimeter was established in 1997 to support clinical trials with data management and statistical exertise. It was a long time ago and while our original mission is still in place, Planimeter became a complex service provider during this 23 years.
Only data and statistics
Though we are a full service CRO, our core business is
- Study design,
- Data management,
- Statistical programing,
- Statistical evalation.
Data management can include even data entry, data cleaning, coding or database migration among different systems.
Our statistical activities cover all usual services like,
- Sample size determination,
- Protocol writing,
- DMP, SAP prepartion,
- SDTM, ADaM mapping,
- SAS programing and
- Statistical report writing.
Beyond clinical trials we are similarly familiar support of post-marketing surveys, epidemiological researches or medical device studies.
eCRF, Data Management and Statistics
Complete data management and statistical support (including the design and implementation of eCRF) of a multinational medical record review in oncology for a Top10 pharma company.
SDTM mapping – including preparation of define.XML and define.PDS – of a phase II clinical trial in haematology for a mid-size pharma company.
Statistical programing and evaluation of a two-way crossover Phase I pharmakokinetic study in pain reduction with co-operation of another CRO for a mid-size pharma company.
We’ve Been in the Market for 23 Years
Planimeter is still a small company with 12 employees and a similar set of contractors. We are very proud that even with this dimensions we could already support 1200+ projects of 500+ clients in 22 countries during our existence of 23 years.
Call For a Quote:
(36) 30 933 8920
During the years, we also developed several web-based solutions to support differenct activities associated with trials, or general pharma activities.
What a web-based solution means?
You have a functionally complete, easy-to-change, well documented and supported system without installing anyting on your local computers.
The systems are available in 7/24, the databases are protected in several ways, you have the maximal comfort with a flexible financial contract.
eCRF (electronic case report form) or EDC (electronic data capture) is our most important tool to support you in data collection. Our solution is fully FDA CFR 21 Part 11 compliant and was used in roughly 10 countries during the last 10 years.
We are regularly audited and what we learned from this audits, that and e-learning system to train and to document the training procedure of our SOPs is a must. Now we share this system with you.
Travelling cost reimbursement
In early phases the voluteers are paid for the collaboration in clinical trials. This is a multi player game: the physician sees the volunteer, the monitor approve the costs, there might be legal limitations, etc. The whole process is managed by our system.
Sales forces effectiveness is a key part in marketing drugs. Our solution is suitable to support the yearly (or longer) planning (strategic approach) with integration of the montly activities (operational approach). You can imagine it as a dashboard, if it helps.