'Kazakhstan' Trends

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Exists to foster the transition towards open market-oriented economies and to promote private and entrepreneurial initiative in the countries of central and eastern Europe and the CIS.
The European Bank for Reconstruction and Development (EBRD) invests in changing lives. Through our financial investments, business services and work on policy reform, we're doing more than ever before to build open, market economies across 3 continents.

Tokayev circumspect on critical minerals.

| Новости Центральной Азии

UTUB.KZ это самые свежие и новые видео, слушайте любимые песни каждый день. Смотреть бесплатно Казахстан, Россия , СНГ .

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Актюбинский областной научно-практический центр

Your daily guide in Caspian Region

Nature-based and cultural tourism, gravity and magnetics for oil exploration, kidney stones, oil statistics, a perpetual geologic calendar, and more

The Voice of Greater Central Asia

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Festival International des Cinémas d'Asie de Vesoul. Festival de films asiatiques chaque année en février.

The official web site of Satrapia Project

Sanjar Madi's Official Web Site. Asian (Kazakhstani actor), "Best Actor" Richmond International Film Festiva '19, known for "Paris Song" (Amre), "The Guardians" (Russian Superhero movie), "The Golden Horde" Series.

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to reduce poverty and hunger, improve human health and nutrition, and enhance ecosystem resilience through high-quality international agricultural research, partnership and leadership in Central Asia and Caucasus

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India is expected to remain one of the fastest-growing major economies in 2026, supported by strong policy measures, favourable demographics and *** digitalisation, even as growth moderates toward long-term trends, according to the Mastercard Economics Institute (MEI). MEI forecasts India's real GDP growth at 6.6 per cent in 2026, easing from the robust 7.8 per cent recorded in 2025. Inflation is projected to rise to 4.2 per cent in 2026 from 2.2 per cent in the previous year, reflecting a normalisation from exceptionally low price pressures. Despite this moderation, India's growth outlook remains resilient, underpinned by domestic policy support and structural strengths. The report notes that front-loaded monetary easing, income tax reforms and the rationalisation of goods and services tax (GST) rates are expected to bolster personal consumption. In addition, targeted export support measures could help mitigate downside risks arising from a challenging global environment. Disinflationary impulses from lower commodity prices and global goods prices are also likely to support India's growth resilience. Structural drivers continue to play a critical role. Digitisation, technological advancement and favourable demographics are positioning India as a key engine of growth among large economies. These factors are also enabling the expansion of global capability centres and strengthening economic activity in Tier 2 and Tier 3 cities, contributing to a broader-based growth model. However, MEI highlights persistent external headwinds. High tariffs imposed by the United States may weigh on labour-intensive sectors such as textiles, gems and jewellery. Tightening immigration norms could also affect India's IT services sector through reduced labour mobility, travel flows and remittances. Progress on the ongoing US-India trade deal will be closely watched, as these developments could influence India's external demand outlook. At the same time, these challenges may accelerate I

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510(k) – Premarket Notification for Medical Device aka PMN AADA – Abbreviated antibiotic drug application ACTD – ASEAN common technical dossier ADR – Adverse drug reaction AE – Adverse event AIM – Active ingredient manufacturer AIMD – Active implantable medical device ANDA – Abbreviated new drug application API – Active *** ingredient AR – Assessment Report (European Union) ASMF – Active Substance Master File ATMPs – Advanced therapy medicinal products BA – Bioavailability BAP – Biotechnology Action Program BIND – Biological investigational new drug BLA - Biologic License Application BWP – Biotech Working Party (EMA) C&P – Chemistry and *** CA – Competent authority CANDA – Computer assisted new drug application CAP – Centrally authorized product CAPA – Corrective action and preventive action CAPLA – Computer Assisted Product License Application CCDS – Company core data sheet CD – Controlled drug CDSCO – Central Drug Standard Organization (India) cGLP – Current good laboratory practice cGMP – Current good manufacturing practice Cl – Total body clearance CLO – Clinical overview CLS – Clinical summary CMC – Chemistry – manufacturing – controls CMP – Certificate of Medicinal Product COA – Certificate of analysis CoFS – Certificate of Free Sale CP – Centralized procedure (European Union) CP – Comparability protocol (USA) CPP – Certificate of *** product CQA – Clinical quality assurance CR – Controlled release CRO – Clinical Research Organization CSI – Core safety information CSP – Core safety profile CSR – Clinical study report (European Union) CT – Clinical trial CTA – Clinical trial application CTA – Clinical trial authorization CTD – Clinical Trials Directive CTD – Common technical document/dossier CTMS – Clinical trial management system CTS – Common technical specification CVM – Center for Veterinary Medicine (US) DACS – Detailed and critical summary DAE – Discontinuation due to an adverse event DDPS – Detailed description of pharmacovigilance system DMF – Drug master file DMS – Document management system DP – Drug product DS – Drug substance DSUR – Development safety update report EA – Environmental assessment EC – Ethics committee eCTD – Electronic common technical document EDMF – European drug master file EDT – Electronic data transfer ENS – Early notification system EPA – Environmental Protection Agency EPL – Effective patent life ePSUR – Electronic periodic safety update report ERB – Ethical review board ESPAR – Executive Summary Pharmacovigilance Assessment Report EUA – Emergency Use Authorization EWG – Expert Working Group EWP – Efficacy Working Party FAR – Final assessment report FMEA – Failure mode and effects analysis GCP – Good clinical practice GDP – Good distribution practice Generic - Generic drug GGP – Good guidance practice GLP – Good laboratory practice GMP – Good manufacturing practice GMP – Good management practice GPP – Good pediatric practice GPP – Good pharmacoepidemiology practice GpvP – Good pharmacovigilance practice GRB – Global Regulatory Board GRP – Good regulatory practice GSL – General sales list GSP – Good statistics practice GVP – Good pharmacovigilance practice HCP – Healthcare professional HEOR – Health economics and outcomes research HREC – Human Research Ethics Committee HTA – Health technology assessment IB – Investigator’s brochure IC – Informed consent ICD – Informed consent document ICSR – Individual case safety report IDE – Investigational Device Exemption IDMP – Identification of medicinal products IEC – Independent ethics committee IM – Issue management IME – Important medical event IMI – Innovative Medicines Initiative IMP – Investigational medicinal product IMPD – Investigational medicinal product dossier IMRDF – International Medical Device Regulatory Forum IMS – Information management strategy INDA – Investigational new drug application (USA) INDC – Investigational New Drug Committee IP – Intellectual property IPO – Intellectual Property Office IPR – Intellectual property rights IQM – Integrated quality management IRB – Institutional review board IRD – International registration document IRN – Incident Review Network IS – Internal standard ISE – Integrated summary of efficacy ISRB – Integrated summary of risk benefit ISS – Integrated summary of safety KIT – Key intelligence topic KM – Knowledge management KOL – Key opinion leader LCM – Lifecycle management LLL – Lifelong learning MA – Marketing authorization MAA – Marketing authorization application (EU) MAH – Marketing authorization holder MAIL – Medicines Act Information Letter (UK) MAL – Medicines Act Leaflet (UK) MDCG – Medical Device Coordination Group MDD – Medical Device Directive MDEG – Medical Device Expert Group MDLO – Medical Device Liaison Officer MDR – Medical device reporting MERS – Multi-agency electronic regulatory system MHRA – Medicines and Healthcare products Regulatory Agency (UK) ML – Manufacturer’s license (UK) MOU – Memorandum of Understanding MRA – Mutual recognition agreement NAP – Nationally authorized product NBE – New biological entity NCE – New chemical entity NCO – Non clinical overview NCS – Non clinical summary NDAC – New Drug Advisory Committee (India) NIMP – Non-investigational medicinal product NME – New molecular entity OD – Orphan drug ODA – Orphan *** Act (USA) ODD – Orphan drug designation OIA – Official action indicated OOS – Out of specification OTC – Over-the-counter *** P&R – Pricing and reimbursement P – *** only P to GSL – *** to General Sales List PA – Product authorization PAI – Pre-approval inspection PAR – Preliminary assessment report PASS – Post authorization safety study PAT – Process analytical technology PDE – Personal daily exposure PER – *** evaluation report PGD – Patient group direction PI – Prescribing information PI – Production information PIL – Patient information leaflet PIM – Product information management (EMA) PIP – Pediatric investigation plan PMS study – Post-marketing safety study PMS – Postmarket(ing) surveillance POM – Prescription-only medicine POM to P – Prescription-only medicine to *** PPI – Patient and Public Involvement (UK) PRSPH – Potential serious risk to public health PSMF – Pharmacovigilance system master file PTE – Patent term extension PUMA – Pediatric-use marketing authorization PV – Pharmacovigilance PVAR – Preliminary Variation Assessment Report QA – Quality assurance QbD – Quality by design QC – Quality control QMS – Quality management system QOL – Quality of life QoS – Quality overall summary QP – Qualified person QPPV – Qualified person for pharmacovigilance QRD – Quality review of documents [template] RA – Regulatory affairs RAPS - Regulatory Affairs Professionals Society RCFID – Registration Certificate for Import of Drug RCT – Randomized controlled trial RDE – Remote data entry RDS – Repeat dose study RDT – Rising-dose tolerance REACH – Registration, evaluation, authorization, restriction of chemicals RI – Regulatory intelligence RING – Regulatory Intelligence Network Group rINN – Recommended international non-proprietary name RMM – Risk minimization measure RMP – Reference medicinal product RMR – Reaction monitoring report ROI – Return on investment RoW – Rest of world RP – Responsible person RPS – Regulated product submission Rx – Prescription S+T – Sampling and testing SAG – Scientific Advisory Group SAP – Scientific advice procedure SAWP – Scientific Advice Working Party SI – Statutory instrument SLA – Service level agreement SME – Significant medical event SMF – Site master file SMO – Site management organization SMQ – Standardized MedDRA query SOP – standard operating procedure SPIN – Special interest network SSC – Scientific Steering Committee TAG – Therapeutic Advisory Group TLV – Threshold limit value TOC – Table of contents TOD – Table of decisions TOPRA – The Organization for Professionals in Regulatory Affairs TPP – Target product profile USDA – United States Department of Agriculture VAI – Voluntary action indicated WC – Written confirmation WL – Wholesale dealer’s license WRAC – Worldwide Regulatory Affairs Committee WHO - World Health Organization