We D-tech impex leading manufacturer and exporter of Automobile parts , Agriculture implement parts, tractor parts, engine parts, Earth movers, Combines and all kinds of machinery parts.We are manufacturer of linch pins, R pins, clevis pins, PTO pins, Fuel pipes, Fuel Hoses, Hydraulic hoses, Harrow disc, Hydraulic fittings, Bolts, Nuts, Fastners, Clamps, BRASS components, BRASS Bushes, CNC turned components and Fuel injection parts.we are specialized in sheat metal components , Fuel Filters, Copper and brass washers and Bushes and All types of linkage parts and allied products.we have complete production.process for bolts, Nuts, fastners, U bolts, Wheel bolts, Centre bolts, Pins , King pins, Brake springs, Speed springs, Fuel injection parts and all types of water pump and hoses.
CyGenica Limited
CyGenica is a pioneering biotech startup redefining the intracellular delivery of genomic medicines through its proprietary platform, GEENIE — an engineered protein nanoneedle capable of delivering payloads directly into the cytoplasm, bypassing endocytosis. GEENIE enables safe, efficient, and targeted delivery of a broad range of therapeutic modalities including siRNA, ASOs, CRISPR-Cas, and gene therapy vectors, addressing one of the most critical bottlenecks in the field of genetic medicine. Our mission is to empower next-generation therapies with precision delivery tools that overcome biological barriers, reduce off-target effects, and improve therapeutic outcomes — especially in tissues traditionally considered hard to reach such as the brain and eye. CyGenica has secured strategic collaborations with two top-tier global pharma/biotech partners. In one collaboration, we demonstrated that GEENIE enabled a clinically validated RNAi candidate to achieve equivalent gene knockdown efficacy at 100-fold lower doses — a breakthrough with substantial implications for safety, dosing, and cost. Our initial in vivo proof-of-concept (POC) studies demonstrated tissue-specific targeting using GEENIE conjugated to a cytotoxic payload (Maytansine) in glioblastoma models, as well as HER2-gastric cancer tumor xenografts. While these programs validated the platform’s targeting and delivery capabilities, we have strategically pivoted toward higher-value opportunities in CNS and ocular indications, where GEENIE’s unique delivery mechanism offers clear differentiation and unmet need. CyGenica holds four granted patents (2 in the U.S., 1 in Europe, and 1 in Japan), protecting the core GEENIE technology. As we scale our partnerships and pipeline, we are actively seeking collaborators across therapeutic areas to co-develop or license delivery-enabled programs powered by GEENIE.
CuraTeQ Biologics
(a wholly owned subsidiary of Aurobindo Pharma Ltd.) is an biopharmaceutical company headquartered in Hyderabad, India. Our vision is to improve the wellbeing of patients suffering from debilitating illnesses by providing them access to high quality and cost-effective biosimilars. CuraTeQ has a development pipeline of 14 biosimilars with a focus on oncology and immunology, of which, three products have been filed with EMA, one product has been filed with MHRA, and four more products are in global phase 3 clinical trials. – ®, (Bevacizumab biosimilar), has received MHRA approval. – ®, (Pegfilgrastim biosimilar), has received EMA approval. – ®, (Filgrastim biosimilar), has received EMA approval. – ®, (Trastuzumab biosimilar), has received CHMP positive opinion, and CDSCO approval in India. : – , our synthetic peptide API manufacturing arm is a US FDA certified facility. We have filed 14 DMFs with the US FDA, contributing to 6 ANDA approvals and 2 CEP approvals. – : we offer a wide spectrum of CDMO services across biologics, peptides, and oligonucleotides including sterile drug product contract manufacturing at our affiliate .
CRQA
CRQA: Your Trusted GxP Compliance and Regulatory Consulting Partner Company: CRQA (Compliance, Regulatory & Quality Assurance) Headquarters: Noida, Uttar Pradesh, India (Office No. 602, 6th Floor, Tower B, B8 Noida One, Sector 62) Website: www.crqa.in Contact: bd@crqa.in | +91 98100 68241 Tagline: GxP Compliance: We have got you covered Who We Are CRQA is an independent, specialized auditing and regulatory consulting organization headquartered in New Delhi/Noida, India. Unlike large contract research organizations (CROs) that offer quality assurance as an add-on, CRQA was built exclusively around GxP compliance — making regulatory excellence our sole focus, not a side offering. Registered with Dun & Bradstreet, ISO 13485 & ISO 9011:2015 certified, and recognized as an MSME, CRQA has positioned itself as a credible and conflict-free compliance partner for pharmaceutical companies, biotechnology firms, clinical research organizations, medical device manufacturers, and healthcare institutions worldwide. Global Reach CRQA operates across more than 60 countries and delivers its services in 30 languages, making it one of the most geographically diverse independent GxP auditing firms in the world. Our network of Auditors spans: • Asia: India, Japan, China, Southeast Asia, including major Indian cities — New Delhi NCR, Noida, Gurgaon, Mumbai, Pune, Bangalore, Chennai, Hyderabad, Kolkata, Ahmedabad, Vadodara • Americas: United States, Latin America • Europe: EU countries, UK • Middle East & Africa • Australia & Oceania This wide geographical presence enables us to deploy region-based auditors who understand local regulatory environments — reducing travel costs and turnaround time for our clients. Why CRQA? — The Value Proposition CRQA was founded to address a critical gap in the pharmaceutical services industry: the absence of a dedicated, independent auditing agency free from conflicts of interest. Key advantages of working with CRQA: ✔ No conflict of interest — CRQA is purely an auditing and consulting firm; we do not run clinical trials or offer CRO services, ensuring full objectivity in every audit. ✔ Specialized expertise — Our auditors are seasoned professionals with deep GxP knowledge, offering a level of focus that generalist CROs cannot match. ✔ Cost efficiency — With locally based auditors across 60+ countries, clients benefit from significant cost savings on travel and logistics. ✔ Better sponsor–CRO relationships — By outsourcing audits to CRQA rather than using competitor CROs, sponsors can maintain neutral, healthy vendor relationships. ✔ Holistic compliance perspective — Our external auditors provide an unbiased, big-picture view of a client’s systems, identifying gaps and improvement opportunities that internal teams may overlook. Services Portfolio CRQA provides a comprehensive suite of GxP auditing and regulatory consulting services: Clinical & Research Compliance • GCP (Good Clinical Practice) Audits and Services • GCP Consultancy • Mock Inspections • BA/BE (Bioavailability/Bioequivalence) CRO Audits • Remote GCP and Pharmacovigilance Audits • Vendor Audits • Study Audits Manufacturing & Distribution Quality • GMP (Good Manufacturing Practice) Audits and Services • GDP (Good Distribution Practice) Compliance • GLP/GCLP (Good Laboratory/Clinical Laboratory Practice) Audits • Pharmaceutical Quality Management Services Pharmacovigilance & Drug Safety • Pharmacovigilance Audits • QPPV (Qualified Person for Pharmacovigilance) Services • Global Pharmacovigilance Outsourcing Services Medical Devices • Medical Device Regulatory Audits and Consulting • ISO 13485 Quality Management System Support Regulatory Affairs & Strategy • Regulatory Pathway Consulting Services • Global Pharmaceutical Outsourcing Services • Dossier Submission Support (Feasibility to Filing) • Qualified Person (QP) Services in Europe Technology & Systems Compliance • Computer System Validation (CSV) • Compliance Training on 21 CFR Part 11 Quality Systems & SOPs • Quality Management and Compliance Systems • SOPs Development and Review Training & Education • Online Training and Workshops • Ethics Committee / IRB Training • Compliance Training Programs Key Clients CRQA has earned the trust of a diverse global clientele, including recognized names across pharma, biotech, medical devices, and healthcare and have worked with wide range of pharma, biopharma and medical device clients from USA, Europe, India. Certifications & Recognition • D-U-N-S Registered (Dun & Bradstreet Verified) • ISO 13485 Certified (Medical Devices Quality Management Systems) • ISO 9001 : 2015 • MSME Recognized (Government of India) Our Differentiator at BIO USA At a conference where partnerships are forged and life sciences innovation meets business strategy, CRQA stands out as the go-to independent partner for: • Pharma and biotech companies entering new markets who need local regulatory audit support • CROs and sponsors seeking objective, third-party GxP compliance evaluations • Medical device companies needing ISO 13485 audits and regulatory consulting • Global life sciences firms looking for cost-effective, scalable compliance solutions across multiple geographies Whether you are preparing for an FDA, EMA, or CDSCO inspection, building your quality management infrastructure, or seeking ongoing pharmacovigilance oversight — CRQA delivers expert, independent, and conflict-free compliance support. Connect With Us at BIO USA kshahani@crqa.in +91 98100 68241 www.crqa.in LinkedIn: CRQA India CRQA — GxP Compliance: We Have Got You Covered.
Crown Decor
Tabillo, a part of Crown Decor, the flagship Royale Touché Laminates, is a $100 mn company with over 45 years of experience, we are the pioneers and largest manufacturer and exporter of High Pressure Laminates (Interior and Exterior) from India. Our factory located at Ahmedabad, has a production capacity of 20 million sq. mtrs per annum, produces a wide array of products for varied applications like – Table Tops for indoor, outdoor and kitchen HPL Compacts for Toilet Cubicles, Lockers and Outdoor Furniture Compact Sheets for exterior applications like facades, fences, pergolas, gates and many more…. HPL Deck for outdoor applications Decorative Laminate Sheets (over 700 colors and 100 finishes) We have an exclusive range of HPL (High Pressure Laminate) Sheets and Table tops which is branded as “TABILLO” which is adorned with versatile features, like Scratch Resistant, Graffiti Resistant, Flame Retardant, Anti-Bacterial, Anti-Microbial, Solvent Resistant, Impact Resistant, have optimal light fastness and are Easy to Clean & Install. Further, with exports to more than 60 countries around the globe, we serve all the major markets like Europe, USA, UK, Australia, Hong Kong, Singapore, Malaysia, Africa and Middle East and have established credentials for our table tops since years. We also have our warehouse in Singapore, Netherlands and Poland (UK, USA, FRANCE opening soon) to facilitate the shipments and smaller requirements.
Crescent Foundry Co. Pvt. Ltd.
Founded in 1982, Crescent is a global leader in casted counterweights & machined castings, delivering 205,000 tons via 4 advanced Indian facilities. We offer end-to-end solutions-design, tooling, machining, top coating, packaging and warehousing in the USA, Europe, & Middle East. Our products range from 1 lbs – 30,000lbs . With SAP®, Magmasoft®, Faro® scanning, ESG-rated by EcoVadis, we ensure quality, compliance & smooth global supply to OEMs.
Credible Planning, Jalson Business Solutions
PACE is the most comprehensive SaaS platform that allows users to plan, track and optimize clinical trials/portfolios of any complexity deterministically or stochastically (including cohort & slot modelling, customized site activation, seasonality impact on enrolment & more). PACE forms a bridge connecting feasibility & operational teams to collaborate and efficiently manage country selection, study site activation planning, enrolment forecasting & actual performance-based reforecasting.