Check out this video: "TO in action" spark.adobe.com/video/QawT4Gdg…
Last day to catch @observer_tech at booth #406 of SCDM 2018 Annual Conference. 23-26 Sept 2018, Seattle, Bellevue. tech-observer.com/cro tech-observer.com/staffing #SCDM2018
Tech Observer is exhibiting at the SCDM Annual Conference (scdm2018.org) in Seattle- Bellevue this September. Visit booth #406 to discover more about our work. Find out how our data managers can help your research at tech-observer.com/cro/data-manag…
Tech Observer Staffing is expanding to serve you better! Find out how we can support your staffing needs. Visit our website at tech-observer.com/staffing or write to us: staffing@tech-observer.com Tech Observer Staffing. Staffing specialist for US companies since 2005.
Whether you are looking for a career change or staffing solutions in Pharmaceutical, IT, Finance, Tech Observer Staffing can help you. Explore the possibilities with us today! Visit our website at tech-observer.com/staffing or write to us: staffing@tech-observer.com
We delivered our 40th article recently (lnkd.in/ffuKvC9). The article about REVIDA study was published in Current Medical Research Opinion.
We are making Complex Simple! #VisualAbstract #medicalwriting #scientificpublications
120 clinical databases & counting! Tech Observer Data Management💪#datamanagement #databases lnkd.in/fCZmHdi
We have managed over 120 clinical databases in more than 20 therapeutic areas. Our electronic data capture system is serving 500+ users in over 20 countries. @observer_tech #DatabaseManagementandMaintenance
We pride ourselves on our ability to provide innovative quality solutions to meet clinical challenges, all delivered RIGHT ON TIME ! #CRO
Let's join our hands this #worldhemophiliaday #supportthecause #beinghuman fb.me/12LCvWl35
Let's join our hands this #worldhemophiliaday #supportthecause #beinghuman fb.me/4FNJIoo4p
(contd)... thus equipping them to design and implement customized and efficient solutions to meet any indigence in clinical research. #cro
(contd).... Pharmacology, Computer Sciences, and Statistics/Biostatistics, who have undergone cross training across domains....(contd) #cro
Our expert team includes skilled group of research professionals holding degrees and certifications in Medicine,... fb.me/4TtIjGd8C
Our employees are excited about what they do and are recognized for their high standards of quality and integrity. #cro #clinicaltrials
(contd)....and commitment for high performance. #cro #clinicaltrials
We've brought together a group of talented people, each with his or her experiences, skill set and imagination,... fb.me/1ckgyjSHn
We encourage our clients to think of us as ‘Service Partners’ who are committed to accelerating and adding value... fb.me/34uYV2rWD
We encourage our clients to think of us as ‘Service Partners’ who are committed to accelerating and adding value... fb.me/6esYCFo6n
()cont..Clinical Study Material Accountability and Site Termination. #cro #clinicaltrials #sas
Budget and Contract Negotiation, Investigator Meeting Planning and Presentation, Site Personnel Training, Interim Site Monitoring #cro
Our Clinical Monitoring services include: Site Identification, Site Qualification and Initiation..()contd #sas #cro #clinicaltrials
()contd...real-time data accessibility and centralized tracking and management of procedures. #cro #clinicaltrials
Our CRAs are both office and regionally based and are experienced in numerous therapeutic areas across drug, biologic and device trials.#cro
We provide comprehensive site monitoring and management, including the assurance of protocol compliance, accurate... fb.me/16RxUIbKQ
()contd...personal relationships with a high level of trust and confidence with all our customers. #cro #clinicaltrials #clinicalresearch
()contd..., consistently retrieving high quality, on-time data. #cro #clinicaltrials #clinicalresearch.
Our monitoring activities are conducted in accordance with ICH GCP compliance and data integrity during each site visit, () contd #cro
Our CRAs are assigned to specific sites for the duration of the study to provide consistent support for sites. #cro #clinicaltrials
Our Clinical Research Associates (CRAs) act as the liaison between the sites and the study team. #cro #clinicaltrials
For more updates follow us on twitter. To follow twitter.com/observer_tech fb.me/T5GckzwB
Tech Observer provides comprehensive site monitoring and management, including the assurance of protocol... fb.me/zgYcilPi
At Tech Observer, client satisfaction is held at premium. By following some of the most stringent and efficient... fb.me/7fcwKNCFr
Resource, based at a Tech Observer office is assigned to sponsor, who provides work delegation and Clinical Data Management Systems. #cro
We have developed and implemented a functional sourcing approach over the past years allowing sponsors to... fb.me/2nDh2LQxa
We Understand client requirements more completely, communicate with candidates more effectively and fill jobs more swiftly. #clinicaltrials
With our finely tuned requirement-to-resource matching procedure, we provide our clients with professionals who match their needs. #cro
We at Tech Observer employ a unique and effective recruiting strategy, which has the capability to reach not only... fb.me/3RSz9iu3o
Our Services include: Regulatory Consulting, Regulatory Operations, Electronic Submissions/eCTD, Regulatory Agency Liaison & more. #cro
We Produce a submission acceptable to local global regulatory authorities Service Partners. #cro #clinicaltrials
We work closely with you to provide strategic regulatory guidance to: Expedite the compilation and submission of your application. #cro
Our Regulatory Affairs Professionals are dedicated to ensuring the successful submission of your application. #cro #clinicaltrials
Tech Observer’s Regulatory Affairs Professionals are dedicated to ensuring the successful and timely submission... fb.me/10Q7wxmEv
Our clinical writing process involves a sequence of scientific, statistical and quality control reviews at each developmental step. #cro
From the initiation of a project to the final document, Tech Observer maintains a high level of communication with you. #cro #clinicaltrials
Tech Observer’s medical writers work closely with your statistical, medical, regulatory and data management teams... fb.me/3WkmmOREb
....(contd) Good Manufacturing Practice (#GMP). #cro #clinicaltrials #techobserver For more visit tech-observer.com
Our QA team consists of senior auditors with expertise in Good #ClinicalPractice (GCP), Good Laboratory Practice (#GLP)...(contd) #cro
We recognize the importance of quality in all aspects of our research and to this end have a global quality assurance (QA) group. #cro
The ever- increasing regulatory stringency towards drug development, demands quality of the highest level. #cro #clinicalresearch
Quality Assurance (QA) lies at the foundation of good clinical research. #cro #clinicaltrials #techobserver
Quality Assurance (QA) lies at the foundation of good clinical research, and with the ever- increasing regulatory... fb.me/7QWNNmg0F
Our secure and 21 CFR Part 11-compliant EDC system with its intuitive user interface is used to host your studies... fb.me/4XVSGnuEE
At Tech Observer our Pharmacovigilance and Drug Safety group is dedicated solely to collecting, interpreting and... fb.me/19CEI1jDP
[Contd] ..and System Administrators direct and maintain the entire EDC process for our clients. Visit tech-observer.com for more!
[Contd] comprehensive on-line data validation, rapid change management and experienced user support. Connect @ tech-observer.com
Key benefits of our #electronicdatacapture system include rapid deployment, flexible study configuration for all phases of trials [contd]
Our secure & 21 CFR Part 11-compliant EDC system w/ its intuitive user interface is used to host your studies on-line #Electronicdatacapture
[Contd] #Datamanagement services: e. Data entry (double) f. Data clarification, consistency/logic checks and querying #cro #clinicalresearch
[Contd.] #Databasemanagement services: c. Database design and Data Validation plan d. #Quality control testing of database #cro
Some of our #datamanagement services: a. Data Management Plan (Quality Control Guidelines) b. Case Report Form (CRF) Design #cro
Our systems & software platforms are fully validated & comply with ICH Guidelines & current US, EU and Canadian government regulations. #Cro
Our Data Management platforms are based on @Oracle Clinical™ #datamanagement #clinicalresearch #globalcro tech-observer.com
Our #QA process formally assesses compliance with corporate and study-specific #SOPs. #datamanagement #clinicalresearch #cro #clinicaltrials
To ensure integrity and accuracy of study data, our Data Management Staff follow corporate #QC and #QA processes. #datamanegement #Cro
Our industry-standard, validated #SAS and data management system is a guarantee that you'll always be provided with high quality data.
We pride ourselves on our ability to provide innovative quality solutions to meet #clinical challenges, delivered right on time, everytime.
10 years, 5 countries! Our journey has been fast paced and extremely fruitful #clinicalresearch #cro #globalcro
Our offices are spread out across the globe! #brazil #usa #india #china #singapore. #clinicalresearch at it's global best with #techobserver
We provide full-service analytical support across the entire product development cycle. For more: tech-observer.com
We believe in #quality and #perfection! #techobserver is your friendly neighborhood clinical research organisation! tech-observer.com
Brilliant advances #science and #medicine only takes you forward! twitter.com/heshnarayanan/…
Alan Burnett from Cardiff University, Cardiff, UK describes different phases of clinical trials and how they work twitter.com/patientpowereu…
#TechObserver has extensive experience in helping its customers become #CDISC compliant. tech-observer.com
.@JayBradner, NIBR President, weighs in on why the time to commit to drug discovery is now: bit.ly/1RmebXm Retweeted by Tech Observer
Pfizer Invites Public to View and Listen to Webcast of May 3 Conference Call with Analysts on.pfizer.com/1LDVrXr Retweeted by Tech Observer
Around 21,000 employees work in Basel and San Francisco. What do these two cities have in common? Find out: ow.ly/ZQ89x Retweeted by Tech Observer
New article by Gillam & Talioti looks at recent advances in management of #dentinehypersensitivity #oralhealth ow.ly/ZfYFd Retweeted by Tech Observer
Happy to be #CRO partners for some of the Top 10 #pharmaceutical companies @novonordisk @GSK @Roche #clinicalresearchatitsbest
Although #earth is 71% water fresh water is still a limited resource. @observer_tech honors #worldwaterday today.
Stay strong #Brussels. Our prayers go out to you.
10 years is long, but for us it whizzed right past! It's 2016 & #Techobserver has now conquered #southeastasia too!
Pfizer's tofacitinib hits targets in ulcerative colitis trials bit.ly/1pEDhuS Retweeted by Tech Observer
Our team in #Delhi, India celebrates the successful end of a project! #cro #techobserver #clinicalresearch
Here are some amazing #clinicalresearch #TED talks to inspire you today! twitter.com/LillyTrials/st…
.@forte shares some of the top #clinicalresearch TED Talks to motivate and inspire: https://t.co/GC3KU9dHWv
— Lilly Trials (@LillyTrials) March 10, 2016
Want to know more about our Statistical/Clinical SAS expertise? Click right here: tech-observer.com/services1.htm
We're in #China!