- Advanced Biometric Services & Solutions Offered by CRO’s
Ideally, Biometrics technology indicates the authentication procedures of an individual resorting to automatic verification of personal characteristics, like fingers, hand, face, voice, and eyes utilizing geometry, prints and pattern recognition and much more.
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- Advanced Biometric Services in India
In simple terms, Biometrics means Life Measurements and is a branch of medical science that studies the unique physical and physiological human traits to recognize an individual.
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- Advanced Biometric Services in India
In simple terms, Biometrics means “Life Measurements” and is a branch of medical science that studies the unique physical and physiological human traits to recognize an individual.
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- Advanced Biometrics Applications & their Utilities
The scientific study of Biometrics is also known as biometric authentication and includes procedures for identifying behavioural characteristics.
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- Advanced Biometrics Service Platform Offered by CRO’s
The study of biometrics is all about evaluating biological traits.
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- Advanced Biometrics Services By CRO’s
The biometric recognition technologies records unique features of an individual. It also makes use of this data to recognize whether a person is sanctioned to do what he is claiming to do.
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- Advanced Risk Management Solutions
eGestalt’s advanced risk management solutions offer a regular, structured, on-going process of assessing, recording, & managing of risks according to industry standards. Avert the likelihood of a particular threat with our effective risk management techniques.
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- Advanced Services offered by Best Biometrics Companies
Biometrics can be considered as a scientific study of measuring biological traits. In the computer security landscape, biometrics refers to the authentication techniques that depend on quantifiable physical traits that can be checked automatically.
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- Advancements in Biometrics Services
Modern medical science and its treatment modalities have joined hands with advanced technologies to arrive at high-end devices.
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- Biometrics Services – Advanced Facilities Offered by Indian CRO’s
Biometrics is a medical science study discipline and is based on the identification of human cells depending on certain intrinsic behavioural characteristics of a human being.
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- Biometrics Services Offered by CRO’s
India today is a well known name in terms of medical development, clinical trials as well as medical tourism.
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- Biometrics Technology Developments & Advanced Services
The development of identification safety commenced from the advent of password combinations, PIN’s and signatures.
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- Biometrics-Services By CRO’s
The biometric recognition technologies records unique features of an individual. It also makes use of this data to recognize whether a person is sanctioned to do what he is claiming to do.
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- British Columbia Proposes Transitional Rules for Elimination of Harmonized Sales Tax
Canada’s Department of Finance has proposed transitional rules to remove the 12% Harmonized Sales Tax (HST) in British Columbia (BC) and re-introduce Provincial Sales Tax (PST) and Goods and Services Tax (GST).
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- Canada Offers New Tax Credit for Care-givers
Canada has announced a federal tax credit for families which came into effect on January 1, 2012.
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- Clinical Trial Development in India
The modern changing lifestyle and its chronic ailments are the principal reasons why we need better medications and treatment processes.
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- CRN-DRAAS in Demand
Netmagic, which works with more than 100 Elite partners, has announced a partenership with Ingram Micro to expand the reach of its offerings to partners in tier-2 and -3 cities. "We have created standrd product packages that partners can sell. The Netmagic partner program will enable partners who want to add a managed services portfolio and solutions," informs Vijayakumar Kulkarni, senior Manager, Product Management, NetMagic.
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- CRO’s Offered Medical Writing Services
With the medical landscape progressing leaps and bounds, medical writing has evolved as a separate field and so have the medical writers.
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- Croatia's Corporate Tax Law Amendments To Take Effect March 1
Croatia’s parliament passed the amendments related to the Corporate Income Tax Law which is expected to come into effect from March 1, 2012.
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- Dormant Norwegian Companies Disallowed Work Permits
While filing for work permit applications for foreign nationals, Norwegian companies need to be actively carrying on business activities in Norway. The immigration directorate has clarified that no dormant companies can file work permit applications on behalf of foreign nationals.
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- DRaaS in Demand
Disaster recovery as a service (DRaaS) is picking up owing to increased need for regulatory compliance and growing need for business continiuity among organizations.
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- Essential Components of Clinical Trials
Clinical trials can be defined as a set of drug development and medical research procedures that generate data efficacy and safety.
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- Experienced Regulatory Submission Team
The Regulatory Submission Teams at Lotus Labs have the expertise & sound knowledge of regulatory requirements; international norms & experience in interacting with renowned global regulatory bodies enable us to ensure quality & reliable compliance.
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- Experienced Regulatory Submission Team
The Regulatory Submission Teams at Lotus Labs have the expertise & sound knowledge of regulatory requirements; international norms & experience in interacting with renowned global regulatory bodies enable us to ensure quality & reliable compliance.
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- Functions of Regulatory Compliance Services in CRO’s
The Indian subcontinent in the last decade has witnessed multiple developments and advancements in clinical trials and in data and project management.
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- High-End Biometrics Service Portfolio
Biometrics are also described as biometric authentication and includes processes for recognizing humans related to one or more inherent behavioral traits.
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- HIPAA Compliance
Need help to carry out effective HIPAA security compliance? Hanna Global offers you HIPAA privacy compliance assistance that includes health & welfare benefit plans. We also help improve efficiency in health care delivery by standardizing EDI.
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- HIPAA Compliance
Need help to carry out effective HIPAA security compliance? Hanna Global offers you HIPAA privacy compliance assistance that includes health & welfare benefit plans. We also help improve efficiency in health care delivery by standardizing EDI
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- Implications of Clinical Laboratory Quality and Services
Clinical laboratory quality control is a discipline to detect, minimize and correct the deficiencies present in the laboratory’s internal analytical process before the releasing the patient results, to enhance the quality of results that are reported by the laboratory.
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- Importance of Clinical Laboratory Tests
Clinical laboratory tests play an essential role in the detection, diagnosis and treatment of diseases. The clinical laboratory scientists also termed as the clinical laboratory technologists carry out these tests by examining and analyzing the body fluids, cells and tissues.
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- Importance of Clinical Trial Phases
Clinical trials act as the key medical research tool for advancing medical know-how and patient care. These trials are conducted when doctors or medical technicians are not sure whether a new clinical approach is working well with people and is safe.
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- India Introduces E-waste Management Rules for Manufacturers and Consumers of Electronics
The Indian Ministry of Environment & Forest (MoEF) has introduced e-waste management rules for the safe disposal and handling of e-waste (Waste electric and electronic equipments) in order to reduce and recycle e-waste in the country.
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- India Introduces E-waste Management Rules for Manufacturers and Consumers of Electronics
The Indian Ministry of Environment & Forest (MoEF) has introduced e-waste management rules for the safe disposal and handling of e-waste (Waste electric and electronic equipments) in order to reduce and recycle e-waste in the country.
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- Medical Significance of Clinical Trial Stages
Clinical trials are generally used to examine the efficiency and safety of medical treatment devices and drugs.
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- Medical Writing Services Offered By CRO’s
With the medical landscape progressing leaps and bounds, medical writing has evolved as a separate field and so have the medical writers.
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- Mexico - Electronic Reporting of Customs Information Mandatory from March 1
February 10, 2012 - Recent modifications to Mexico’s foreign trade rules make it mandatory for export and import businesses to file information regarding customs transactions electronically.
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- Need for Positive Clinical Research Programs For Better Medical Treatments
Clinical research plays a vital role in the treatment discovery and drug development process. The new era hectic lifestyle has increased the frequency of chronic ailments globally.
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- New Age Uses of Healthcare Biometrics
According to a report Transparency Market Research concentrating on the medical biometrics market estimates that the segment was valued at USD 1.2 billion in 2012 and is calculated to grow at rate of CAGR of 25.9% from 2013 to 2019, to go up to an expected amount of USD 5.8 billion in 2019.
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- Regulatory Compliance | PROLIM
PROLIM Regulatory Compliance centralizes compliance information and documentation, making it easier for enterprise organizations to achieve and maintain compliance with environmental, product safety, medical device other processes and standards on a global balance.
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- Regulatory Compliance Management Solutions
eGestalt’s SecureGRC™ compliance management software provides a comprehensive, scalable regulatory compliance management solution that leverages our unique combination of strengths in product development, content and product data management and process controls
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- Regulatory Services and Audit Compliance
The dedicated team for regulatory services and audit compliance at Lotus Labs is backed by in-depth knowledge of local regulatory procedures and effective liaison with various regulatory agencies, ensuring efficiency in the clinical trial approval process.
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- Regulatory Services and Audit Compliance
The dedicated team for regulatory services and audit compliance at Lotus Labs is backed by in-depth knowledge of local regulatory procedures and effective liaison with various regulatory agencies, ensuring efficiency in the clinical trial approval process.
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- Regulatory Services and Audit Compliance
The dedicated team for regulatory services and audit compliance at Lotus Labs is backed by in-depth knowledge of local regulatory procedures and effective liaison with various regulatory agencies, ensuring efficiency in the clinical trial approval process.
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- Regulatory Submission
The Regulatory Submission Teams at Lotus Labs are committed to ensuring best-in-class regulatory submissions with sound knowledge of regulatory requirements, international norms &interacting with global regulatory bodies enable us to ensure quality & reliable compliance with regards to study submissions. The regulatory submission activities include Formulation of regulatory strategies, Compilation of the clinical trial application, Submission and follow-up of the application, Response to regulatory agency queries, Procurement of drug import licenses, Procurement of NOC for export of biological samples and many more as required by the sponsor.
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- Regulatory Submission
The Regulatory Submission Teams at Lotus Labs are committed to ensuring best-in-class regulatory submissions with sound knowledge of regulatory requirements, international norms &interacting with global regulatory bodies enable us to ensure quality & reliable compliance with regards to study submissions. The regulatory submission activities include Formulation of regulatory strategies, Compilation of the clinical trial application, Submission and follow-up of the application, Response to regulatory agency queries, Procurement of drug import licenses, Procurement of NOC for export of biological samples and many more as required by the sponsor.
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- Regulatory Submission
The Regulatory Submission Teams at Lotus Labs are committed to ensuring best-in-class regulatory submissions with sound knowledge of regulatory requirements, international norms &interacting with global regulatory bodies enable us to ensure quality & reliable compliance with regards to study submissions. The regulatory submission activities include Formulation of regulatory strategies, Compilation of the clinical trial application, Submission and follow-up of the application, Response to regulatory agency queries, Procurement of drug import licenses, Procurement of NOC for export of biological samples and many more as required by the sponsor.
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- Regulatory Updates: Denmark, Malaysia, Germany, Ireland & Japan
The Danish Government plans to eliminate special tax rules on employee share ownership plans and individual share-based remuneration plans. German government introduces a new tax return form
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- Services Offered By Indian CRO’s
India has been successfully able to provide cost savings of 50 to 60 percent in clinical trials. With the research discovery acquiring approximately one-third of the R&D expenses of the western medical industry, outsourcing to lesser expense countries is a wise move.
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- Spain Introduces New Tax and Administrative Measures to Reduce Public Deficit
In order to reduce public deficit this year, the Spanish government has introduced provisional measures to the Corporate Income Tax. Read the complete Press release to know more about the introduced provisional measures.
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- Understanding the Fundementals of Clinical Trials & its Phases
Clinical trials are medical researches that are carried on utilizing human participants by researchers in medical schools, government labs, or by pharmaceutical manufacturers in order to review how a certain medical device, a new drug, therapy, diagnostic tool, treatment or a type of prevention is working to enhance patient health, cure ailment and enhance the overall quality of life.
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