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menu home -- industry solutions industry solutions areas of application areas of application areas of application preclinical send clinical genetic toxicology bioinformatics areas of focus browse our solutions industries we serve browse industries on-demand demos & presentations request form case studies download form about instem about instem what we do leadership team instem worldwide partnering with instem careers investor centre customer center products & delivery products & delivery products products products acis™ animal care information system alphadas® early phase clinical ames study manager™ comet assay iv™ cyto study manager logbook™ eln notocord-hem™ safety pharmacology solution provantis® preclinical samarind rms for rim sorcerer colony counter™ send explorer® - new! submit™ send sendtrial™ - new! services services services data management instem cloud knowledgescan target safety assessment regulatory information management send data conversion sendready™ consulting solution deployment validation on-demand demos & presentations request form case studies download form already an instem client? visit the instem customer center news & events contact us the benchmark for regulatory information management the samarind rms suite is a fully integrated software solution that has been purpose built to mirror the processes associated with acquiring and maintaining product licenses. samarind rms provides a smarter way to manage your medical product information. using samarind rms, you only need to enter data once and can reuse it as many times as required. for example an ‘inn’ can be entered once and reused for all related ima submissions, renewals, variations, psurs and xevmpd submissions. this concept applies to all key data held within the system and is proven to streamline workflows and help to increase data quality. our pragmatic approach to systems design and implementation means that our customers can manage their licenses smoothly and efficiently, safe in the knowledge that our single-place-of-truth™ approach for regulatory affairs professionals delivers a complete end-to-end system. our features include: a secure regulatory information management (rim) system with planning, tracking, automated alerts and comprehensive reporting facilities an electronic document management system (edms) with version control, template creation and the ability to link to external document management systems such as documentum™ or sharepoint™ an optional ectd module for dossier creation and maintenance (vnees & nees are also supported) an optional evmpd module for automated maintenance of data required by the ema’s extended medicinal product dictionary, xevmpd with a clear roadmap for idmp a med info addition, for quick and easy logging of medical information queries, with links to the associated products elsewhere in the system as necessary medical device registration solution with project management support and fda udi generation a drug safety module, handling pharmacovigilance requirements project management solution, a managers tool linking your tasks & data key benefits increased administrative efficiency, allowing timely response to critical deadlines improved global regulatory communications via information sharing through the medicinal product life cycle improved product launch planning, helping to maximise product revenue transparency of global licensing activities and current status, keeping tight and timely product control greater security of license data, supporting better information control increased compliance via secure access, audited activities and permissions reduced global product portfolio maintenance costs via single data entry, extensive reporting and alerts maximizes the potential earnings of your licenses download a fact sheet samarind rms overview rim for medical devices rim for generics rim for drug safety regulatory information management the core of samarind rms is its regulatory information management database. this has been carefully structured to allow you to accurately record and maintain all your medicinal product information throughout its lifecycle. the samarind rms windows software application provides the security, flexibility and ease of use that your regulatory affairs team needs to meet its regulatory and commercial obligations. at-a-glance visibility of all the products in your portfolio; a secure central repository of all your product documentation, from smpcs and pils to psurs and business contracts ; sophisticated administrator-configurable role-based user permissions, for flexible security; event tracking for drug licensing applications, variations, psurs and renewals; record information about key partners e.g. api manufacturers and qc testing sites; time stamped historical audit of all previous submissions and variations; dashboard kpi's & system generated alerts at key stages; all data is contained within the same sql database for security, robustness and performance; extremely flexible and user friendly search and reporting facilities. fact sheet fact sheet medical devices medical devices the samarind rms medical device solution offers one of the most efficient and practical ways to manage all of your device registration information in one place. our proven, intuitive software has been designed to help our customers more easily manage their licenses with complete confidence. our pragmatic approach to systems design and implementation means that our customers can manage their licenses smoothly and efficiently, safe in the knowledge that our single-place-of-truth™ approach for regulatory affairs professionals delivers a complete end-to-end system. the samarind rms solution is well known in the marketplace as a high quality, sophisticated, user-friendly and well-architected application. our solutions are in use every day by customers around the world and are supported by a level of customer service that is setting a new benchmark for client satisfaction within the life sciences. regulatory standards – it’s what we do… the samarind rms solution leads the way on xevmpd data management and processing as well as providing full support for the fda’s udi standard. our unique database structure means that the transition to idmp will be just that – a smooth transition. instem has been supplying world-leading solutions to the life science community for more than 30 years and is well versed in all aspects of regulatory data capture, reporting and management in support of the industry’s processes. as a stable publicly traded corporation, instem’s trusted services and solutions are supporting drug developers, medical device organizations, contract laboratories, consultants, universities, government agencies and leading health institutes in their missions. once connected, always connected. once clients become proficient users, instem becomes an extension of their business ensuring they receive the highest amount of value from our integrated software. through our relationship managers and value-added support tools, clients have access to a wealth of resources and support so they stay focused on their science, not their software. our solutions work independently or together, all designed to help clients bring their life enhancing products to market faster. key benefits fully integrated end-to-end management for marketed medical devices full electronic record of regulatory communications provides one “single place of truth” to manage all product registrations in all regions more commercial insight due to availability of integrated global regulatory data for analysis supports multi-disciplinary, global product launches increased administrative efficiency from managing a single integrated set of licence & product data provides different risk classification schemes in each market integrated, secure edms with archiving capabilities delivers effective global management of product lines though powerf

URL analysis for samarind.co.uk

https://www.instem.com/solutions/samarind-rms///about/
https://www.instem.com/solutions/samarind-rms///privacyshieldpolicy/
https://www.instem.com/solutions/samarind-rms///solutions/genetic-toxicology/cyto-study-manager.php
https://www.instem.com/solutions/samarind-rms///contact/locations.php
https://www.instem.com/solutions/samarind-rms///solutions/genetic-toxicology/comet-assay.php
https://www.instem.com/solutions/samarind-rms//../../contact/video-requests/index.php
https://www.instem.com/solutions/samarind-rms///products/data-management.php
https://www.instem.com/solutions/samarind-rms///about/leadership-team.php
https://www.instem.com/solutions/samarind-rms///about/partnering-with-instem.php
https://www.instem.com/solutions/samarind-rms///solutions/
https://www.instem.com/solutions/samarind-rms///solutions/knowledgescan/index.php
https://www.instem.com/solutions/samarind-rms///solutions/genetic-toxicology/sorcerer-colony-counter.php
https://www.instem.com/solutions/samarind-rms///about/careers.php
https://www.instem.com/solutions/samarind-rms///about/instem-worldwide.php
https://www.instem.com/solutions/samarind-rms///solutions/acis/index.php

Whois Information

Whois is a protocol that is access to registering information. You can reach when the website was registered, when it will be expire, what is contact details of the site with the following informations. In a nutshell, it includes these informations;

Domain name:
samarind.co.uk

Registrant:
Samarind Ltd

Registrant type:
UK Limited Company, (Company number: 2105894)

Registrant's address:
Parkway Business Centre
Parkway, Deeside Industrial Park
Deeside
Flintshire
CH5 2LE
United Kingdom

Data validation:
Nominet was able to match the registrant's name and address against a 3rd party data source on 13-May-2014

Registrar:
Fasthosts Internet Ltd [Tag = LIVEDOMAINS]
URL: http://www.fasthosts.co.uk

Relevant dates:
Registered on: 12-Jun-1998
Expiry date: 12-Jun-2018
Last updated: 13-May-2017

Registration status:
Registered until expiry date.

Name servers:
ns0.ukfast.net
ns1.ukfast.net

WHOIS lookup made at 09:33:41 22-Sep-2017

--
This WHOIS information is provided for free by Nominet UK the central registry
for .uk domain names. This information and the .uk WHOIS are:

Copyright Nominet UK 1996 - 2017.

You may not access the .uk WHOIS or use any data from it except as permitted
by the terms of use available in full at http://www.nominet.uk/whoisterms,
which includes restrictions on: (A) use of the data for advertising, or its
repackaging, recompilation, redistribution or reuse (B) obscuring, removing
or hiding any or all of this notice and (C) exceeding query rate or volume
limits. The data is provided on an 'as-is' basis and may lag behind the
register. Access may be withdrawn or restricted at any time.

  REFERRER http://www.nominet.org.uk

  REGISTRAR Nominet UK

SERVERS

  SERVER co.uk.whois-servers.net

  ARGS samarind.co.uk

  PORT 43

  TYPE domain

OWNER

  ORGANIZATION Samarind Ltd

TYPE
UK Limited Company, (Company number: 2105894)

ADDRESS
Parkway Business Centre
Parkway, Deeside Industrial Park
Deeside
Flintshire
CH5 2LE
United Kingdom
Data validation:
Nominet was able to match the registrant's name and address against a 3rd party data source on 13-May-2014

DOMAIN

  SPONSOR Fasthosts Internet Ltd [Tag = LIVEDOMAINS]

  CREATED 1998-06-12

  CHANGED 2017-05-13

STATUS
Registered until expiry date.

NSERVER

  NS0.UKFAST.NET 81.201.128.133

  NS1.UKFAST.NET 81.201.143.133

  NAME samarind.co.uk

DISCLAIMER
This WHOIS information is provided for free by Nominet UK the central registry
for .uk domain names. This information and the .uk WHOIS are:
Copyright Nominet UK 1996 - 2017.
You may not access the .uk WHOIS or use any data from it except as permitted
by the terms of use available in full at http://www.nominet.uk/whoisterms,
which includes restrictions on: (A) use of the data for advertising, or its
repackaging, recompilation, redistribution or reuse (B) obscuring, removing
or hiding any or all of this notice and (C) exceeding query rate or volume
limits. The data is provided on an 'as-is' basis and may lag behind the
register. Access may be withdrawn or restricted at any time.

  REGISTERED yes

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