BIOSTATISTIC

AND CLINICAL

    PROGRAMMING

One of the main components of the analysis is the statistical analysis plan (SAP). This plan ensures that the analyses to evaluate all planned study hypotheses are conducted in a scientifically valid manner and that all decisions are documented. It also provides detail on how the results will be presented and reported. 

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BUSINESS

        ADVISORY

EIEN Biosciences  has a vision of building a ramp & partnering with growing, ambitious and technically focused  pharmaceutical, medical services,medical industry organisations including innovative startups and 

professionals , requiring the current day  Business Management models & scaling up solutions in order to success at game changing  & also world changing ideas to fruition

MEDICO

     MARKETING

          SERVICES

 

  • Pre-launch and launch marketing strategies

  • Branding and product positioning strategies

  • CME program planning and development

  • Advisory board and expert panel management

  • Scientific event management including medical conferences, launch events, CME meetings, satellite symposia, training workshops and seminars

  • Disease education programs for healthcare professionals and patients

  • With best of translation services in India and medical expertise, there is an advantage of our end-to-end localization, translation and medical technical services to take your business to the global platform. Some of our most compelling benefits include:

  • Committed support of professionally qualified in-house and contracted native translators, subject matter experts and localization engineers.

  • Highly competitive and affordable services.

  • Professional approach to ensure delivery on time.

TRANSLATION

      SERVICES

OUR

TRIAL PLANNING, DESIGN,

PROJECT MANAGEMENT

MEDICAL WRITING

AND REGULATORY

DATA MANAGEMENT 

SERVICES

CLINICAL PROGRAMMING

MEDICO MARKETING SERVICES

BUSINESS ADVISORY

DATA

   MANAGEMENT

        SERVICES

Striking Features of EIEN Electronic Data Capture (EDC) includes:

  • Electronically Capture the data into e-CRF

  • Allows to generate barcode for IP dosing and Sample collection

  • Allows subject management

  • Allows Randomization or Treatment assignment

  • Real time data capturing

  • Visit wise scheduling

  • Capturing data using barcode gun reader

  • User Rights Specific Data Entry

MEDICAL

    WRITING

Eien believes in quality submission leading to a promising approval.

Eien has routinely provided expertise for the following document types:

  • Clinical Protocols

  • Clinical Protocol amendments

  • Case Report Forms

  • Informed Consent

  • Investigator Brochures

  • Clinical Study Reports (CSRs)

Given the costly drug development process and the limited resources of biopharmaceutical companies developing an early regulatory strategy starting well before clinical trials are initiated is extremely important for the success of a company.

REGULATORY

       SERVICES

 
 
 
 
 
 
 
 
 
 

TRIAL

    PLANNING,

          DESIGN AND

       PROJECT  MANAGEMENT

A robust trial design is essential to ensure a successful outcome. The trial design should be considered before developing the protocol.

A well-documented study plan will facilitate the process of developing ethics committee and R&D approvals and any necessary regulatory approvals.

 

TRANSLATION SERVICES

Disclaimer: Eien Bioscience Private Limited Does Not Take Ownership Of The Images Displayed On This Website. They Are Strictly Shown As An Example To Address The Kind Of Respective Service We Provide.

@COPYRIGHT EIEN-BIOSCIENCE 2017