RECON Lite

We make it easy..

About RECON Lite

The clinical trial phase is very important for any pharma company, various parallel activities and assignments to be completed in order to meet compliance and monitoring the entire phase.

RECON Lite is a specially designed solution to help pharma companies to reconcile their database.

RECON Lite reconciles Data from the Safety database and clinical trial databases and process data in order to generate various analysis or regulatory reports submitted to authorities.

.

Problems we solve

DB reconciliation

Reconciliation between Safety Database and Clinical Database.

Process Automation

Key fields of clinical DB gets reconciled automatically with the safety database .

Design Process SOP

Design and develop SOP process defining dependencies and inclusions.

No Data Loss

Recon Lite automates Data from Clinical DB to Safety DB without data loss.

Send us questions.



    RECON Lite Features

    Automated

    Recon lite is a fully automated solution to ensure quick turnaround and timely delivery.

    Accurate

    Recon lite ensures 100% accuracy in data analysis, tabulation and formated reporting.

    Interactable

    Recon lite can be integrated with any existing system or solution with minimum configuration.

    Why RECON Lite?

    5 Star Rating

    RECON Lite has proven track with various pharma companies with 5 Star rating.

    Secure Data

    RECON LIte is powered by latest and secure technology like coud and bigdata.

    Easy to Automate

    With the Help of RECON lite, it is very easy to automate literature data monitoring.

    Regulatory Ready

    RECON lite is a Regulatory ready solution, so huge time and cost save for pharma companies.

    Frequently asked questions

    Yes, RECON Lite is capable collecting data from almost any platform. we can pull data from xls sheet and transform as required. 

    With direct database API, can be done in 4 weeks. Takes 8 weeks otherwise to develop integrations. 

    Yes, we understand your business needs and regulatory requirements. We can customize this solution based on your requirement. 

    Read our blog

    Regulatory

    Electronic submissions for IND Safety Reports to FAERS

    • admin
    • 0 Comments

    Blog Electronic submissions for IND Safety Reports to FAERS Key Highlights Starting June 28, 2021,...

    Read More »

    AI

    Better PV Compliance with Automated Workflows

    • admin
    • 0 Comments

    Blog Better PV Compliance with Automated Workflows Pharma, Biotech, CRO and Life Sciences companies have PV...

    Read More »

    AI

    Artificial Intelligence for ICSR processing

    • admin
    • 0 Comments

    Blog Artificial Intelligence for ICSR processing With the strides taken in technology, we are at...

    Read More »

    TESTIMONIALS

    What Our Client Say About Us

    We trust Olcay for on time delivery and out of box support. 

    25388788904_72d2f5ec6f_z.jpg
    Siara Miller Found & President

      Olcay have been proven partner for all our pharma needs.

      img2.jpg
      John Doe VP Technology

        Olcay is our technology partner for regulatory reports.

        25497478040_140ce47f31_k-1.jpg
        Eva Spice Head - Operations