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Check out this video: "TO in action" spark.adobe.com/video/QawT4Gdg…

Happy Diwali!

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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

Our colleagues from the USA and India office, are looking forward to meeting you at SCDM 2018 Annual Conference. Visit us at booth #406 at SCDM 2018 Annual Conference. 23-26 Sept 2018, Seattle, Bellevue.

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.

Success by design. 7 factors to consider during journal selection.

We are making Complex Simple! #VisualAbstract #medicalwriting #scientificpublications

May this day bring peace, happiness, prosperity, and love to everyone.

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

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(CONTD)...is a guarantee that you will always be provided with data of the highest quality

Our industry-standard, validated SAS and data management system, compliant with ICH GCP guidelines and 21 CFR Part 11 regulations...(CONTD)

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, Pharmacy...(contd)

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, all with the energy..(contd)

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

All of our CRAs have state-of-the-art communications tools in place to provide timely and responsive communications..()contd

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

Our Clinical monitoring team ensures the adherence with standard operating procedures (SOPs) and strives to promote positive...()contd

()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

We provide site monitoring and management, including the data capture, & GCP/ICH compliance at investigative sites.

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 are best known for our Functional Service Provision, we become an extension of your clinical team through a combination of HR solutions

We have implemented a functional sourcing approach over the past years allowing sponsors to leverage our expertise within clinical research.

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 employ a effective recruiting strategy, which has d capability to reach national resource pool as well as the international resource pool

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 medical writing services include clinical and regulatory writing as well as scientific communications and medical writing consultancy.

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

Our medical writers work closely with medical & data management teams 2 deliver accurate & cost-effective documents.

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

A customizable and robust workflow, combined with our data management SOPs seamlessly integrate all of the data management steps. #edc #cro

[Contd] ..and System Administrators direct and maintain the entire EDC process for our clients. Visit tech-observer.com for more!

Our experienced group of Project Managers, Database Managers, Database Coordinators, Data Reviewers.. [Contd]

[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

Our systems, SOPs, and personnel are equipped to manage all 3 methods of data capture, Fax, Paper & EDC

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

. Our team is trained to be experts at #statisticalanalysis #SAS #clinicaltrials and more!

Our team is trained to be experts at #statisticalanalysis #SAS #clinicaltrials and more!

Happy to be #CRO partners for some of the Top 10 #pharmaceutical companies @novonordisk @GSK @Roche #clinicalresearchatitsbest

#HAPPYHOLI to everybody from team #techobserver ! Don't waste water today, save water! 🙂

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!

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…

We're not just Service Providers, we're your #clinical #research organisation partners! #cro

Want to know more about our Statistical/Clinical SAS expertise? Click right here: tech-observer.com/services1.htm

We're in #China!