{"id":3402,"date":"2023-08-12T11:44:26","date_gmt":"2023-08-12T11:44:26","guid":{"rendered":"https:\/\/wptf.themepul.co\/tronix\/?page_id=3402"},"modified":"2025-10-25T07:29:11","modified_gmt":"2025-10-25T07:29:11","slug":"about-us","status":"publish","type":"page","link":"https:\/\/relstate.esy.es\/bmw\/about-us\/","title":{"rendered":"About"},"content":{"rendered":"\t\t
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About > About Us<\/h5>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Established in 1972, by<\/br> Late Dr. Vasant Palkar<\/h4>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Nivedita Chemicals Pvt. Ltd.\u00a0is a 53-year-old company, established in 1972 by Dr. Vasant Palkar. Since 1987, we have been serving the pharmaceutical industry both in India and internationally, delivering high-quality and affordable healthcare drugs\u00a0across the globe.<\/span><\/p>

Our sister concern, Anek Prayog Pvt. Ltd., serves as the exclusive manufacturing site\u00a0for Nivedita Chemicals. The facility is located on approximately two acres of land in Village Dhatav, Roha MIDC, in the state of Maharashtra, India. Meanwhile, Nivedita Chemicals, headquartered in Mumbai, manages the financial, marketing, and R&D\u00a0operations of the business.<\/span><\/p>

Anek Prayog Pvt. Ltd. features state-of-the-art manufacturing facilities\u00a0supported by a robust Quality Management System (QMS). The site is equipped with advanced instruments and equipment, ensuring precision and compliance with international standards. A dedicated manufacturing block for excipients is in place, with an annual production capacity of around 60 MT.<\/span><\/p><\/div>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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We are proud to be the world\u2019s largest manufacturer of Trimetazidine Dihydrochloride\u00a0and the first Asian company\u00a0to receive the Certificate of Suitability (CEP)\u00a0for this product.<\/span><\/p>

Anek Prayog holds multiple prestigious regulatory accreditations. The facility is regularly audited by EU\/EDQM and WHO, and has previously been inspected and approved by USFDA, Korean FDA, and Mexican FDA. Additionally, we maintain ANVISA cGMP certification\u00a0for our products.<\/span><\/p>

We have submitted Drug Master Files (DMFs)\u00a0to regulatory authorities across Europe, South America, South Africa, Korea, Taiwan, Israel, Iran, and East Asia. We provide full technical and regulatory support\u00a0to our customers worldwide.<\/span><\/p>

We have built a strong reputation on the global stage. Along with supplying APIs and excipient to India\u2019s top pharmaceutical companies, we export to more than 25 countries\u00a0across Asia, Australia, Europe, North America, and South America. Currently, exports account for 90%\u00a0of our total turnover.<\/span><\/p><\/div>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Why Us?<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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  • World-Class Manufacturing Facility:<\/strong>\u00a0Our state-of-the-art manufacturing facility and infrastructure have received multiple national and international GMP approvals, ensuring the highest standards of quality, safety, and consistency in every product we deliver.<\/span><\/li>
  • Commitment to Quality and Innovation:<\/strong>We continuously strive to enhance our products in terms of quality, stability, and reproducibility, aligning with customer needs and regulatory expectations. Our goal is to provide affordable and reliable products\u00a0without compromising on excellence.<\/span><\/li>
  • Strong Regulatory and Technical Support:<\/strong>\u00a0Our experienced Regulatory Affairs Team\u00a0provides comprehensive support to customers worldwide. The team is well-versed with the requirements of various global regulatory agencies, ensuring smooth documentation and compliance.<\/span><\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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    • Long-Term Business Relationships:<\/strong>\u00a0We believe in nurturing long-term partnerships\u00a0with our customers and associates. Our strong global network reflects this trust \u2014 exports account for nearly 90%\u00a0of our total turnover.<\/span><\/li>
    • Sustainable and Safe Practices:<\/strong>\u00a0We focus on developing reproducible, efficient, and hazard-free processes, ensuring a safe and sustainable work environment. We are equally committed to environmental protection\u00a0and contributing positively to the community.<\/span><\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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      • Skilled and Dedicated Team:<\/strong>\u00a0Our success is driven by our highly qualified and experienced team, who ensure quality and compliance at every stage of production.<\/span><\/li>
      • R&D Excellence:<\/strong>\u00a0Our R&D department\u00a0synthesizes and characterizes various impurity standards, which we supply to our customers worldwide. Continuous innovation and scientific expertise are at the core of our operations.<\/span><\/li><\/ul>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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        \n\t\t\t\t\t\t\n\t\t\t\t\t\t\tMilestones\t\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/h3>\n\t\t\t\t\n\t\t\t\t\n\t\t\t<\/div>\n\t\t\t\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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        Company\u2019s significant milestones since inception.<\/strong><\/h6>
        Year<\/strong><\/span><\/td>

        Milestones<\/strong><\/span><\/p><\/td><\/tr>

        2024<\/strong><\/span><\/td>

        Audited and approved by ANVISA authorities<\/span><\/p>

        CBPF\/GMP certificate received for Trimetazidine Dihydrochloride and Dexchlorpheniramine maleate<\/span><\/p><\/td><\/tr>

        2013 & 2017<\/strong><\/span><\/td>

        Audited and approved by EU authorities.<\/span><\/p>

        EU-GMP Certificate received for Trimetazidine Dihydrochloride.<\/span><\/p><\/td><\/tr>

        2011<\/strong><\/span><\/td>

        US FDA has inspected and classified our manufacturing facility as acceptable as per USFDA regulatory requirements.<\/span><\/p><\/td><\/tr>

        2009<\/strong><\/span><\/td>

        Audited and approved by Korean FDA (MFDA). <\/span><\/p><\/td><\/tr>

        2008<\/strong><\/span><\/td>

        Maharashtra State Export Award<\/span><\/p><\/td><\/tr>

        2004<\/strong><\/span><\/td>

        Became a WHO-GMP certified company.<\/span><\/p><\/td><\/tr>

        1989-90<\/strong><\/span><\/td>

        Export Award and Certificate of Merit from Chemixcil.<\/span><\/p><\/td><\/tr>

        1987<\/strong><\/span><\/td>

        M.L. Dahanukar Enterpreneurship Award.<\/span><\/p><\/td><\/tr>

        1985<\/strong><\/span><\/td>

        Raigad District Award.<\/span><\/p><\/td><\/tr>

        1981<\/strong><\/span><\/td>

        R&D department is recognized by Department of Scientific and Industrial Research (DSIR),\u00a0 Government of India\u00a0 <\/span><\/p><\/td><\/tr>

        1979<\/strong><\/span><\/td>

        Republic Day National Award for Import Substitute -Vitamin B2-5 Phosphate Sodium<\/span><\/p><\/td><\/tr>

        1979<\/strong><\/span><\/td>

        Anek Prayog Pvt Ltd was founded<\/span><\/p><\/td><\/tr>

        1972<\/strong><\/span><\/td>

        Introduced Vitamin B2-5 Phosphate Sodium, for the first time in India.<\/span><\/p><\/td><\/tr>

        1972<\/strong><\/span><\/td>

        Nivedita Chemicals Pvt. Ltd founded.<\/span><\/p><\/td><\/tr><\/tbody><\/table>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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        \n\t\t\t\t\t\t● To manufacture vital drugs as import substitutes, so that we can become a self-sufficient nation in the realm of medicine and healthcare.<\/br>\n●To ensure customer satisfaction on quality and timely delivery of our products, as per the regulatory and quality standards followed internationally. <\/br>\n● To provide a safe working environment through effective work practices, staff training, enhancement of infrastructure, and the use of<\/br> state-of-the-art technology.<\/br>\n● To meet dynamically changing, diverse consumer needs through supply and marketing of quality products and services.<\/br> \n● To be engaged in continuous Research and Development activities in order to foster innovation in the pharmaceutical industry.<\/br>\n● To develop processes and policies that reflect our corporate social responsibility.
        ● We are committed to continual quality improvement that emphasizes the accountability of every employee for product quality, workplace excellence, and the overall growth of our business.\t\t\t\t\t<\/p>\n\t\t\t\t\n\t\t\t<\/div>\n\t\t\t\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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        \n\t\t\t\t\t\tTo be a preferred healthcare partner for pharmaceutical industries in India, and globally.\t\t\t\t\t<\/p>\n\t\t\t\t\n\t\t\t<\/div>\n\t\t\t\n\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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        About > About Us Established in 1972, by Late Dr. Vasant Palkar Nivedita Chemicals Pvt. Ltd.\u00a0is a 53-year-old company, established in 1972 by Dr. Vasant Palkar. Since 1987, we have been serving the pharmaceutical industry both in India and internationally, delivering high-quality and affordable healthcare drugs\u00a0across the globe. Our sister concern, Anek Prayog Pvt. Ltd., serves as the exclusive manufacturing site\u00a0for Nivedita Chemicals. The facility is located on approximately two acres of land in Village Dhatav, Roha MIDC, in the state of Maharashtra, India. Meanwhile, Nivedita Chemicals, headquartered in Mumbai, manages the financial, marketing, and R&D\u00a0operations of the business. Anek Prayog Pvt. Ltd. features state-of-the-art manufacturing facilities\u00a0supported by a robust Quality Management System (QMS). The site is equipped with advanced instruments and equipment, ensuring precision and compliance with international standards. A dedicated manufacturing block for excipients is in place, with an annual production capacity of around 60 MT. We are proud to be the world\u2019s largest manufacturer of Trimetazidine Dihydrochloride\u00a0and the first Asian company\u00a0to receive the Certificate of Suitability (CEP)\u00a0for this product. Anek Prayog holds multiple prestigious regulatory accreditations. The facility is regularly audited by EU\/EDQM and WHO, and has previously been inspected and approved by USFDA, Korean FDA, and Mexican FDA. Additionally, we maintain ANVISA cGMP certification\u00a0for our products. We have submitted Drug Master Files (DMFs)\u00a0to regulatory authorities across Europe, South America, South Africa, Korea, Taiwan, Israel, Iran, and East Asia. We provide full technical and regulatory support\u00a0to our customers worldwide. We have built a strong reputation on the global stage. Along with supplying APIs and excipient to India\u2019s top pharmaceutical companies, we export to more than 25 countries\u00a0across Asia, Australia, Europe, North America, and South America. Currently, exports account for 90%\u00a0of our total turnover. Why Us? World-Class Manufacturing Facility:\u00a0Our state-of-the-art manufacturing facility and infrastructure have received multiple national and international GMP approvals, ensuring the highest standards of quality, safety, and consistency in every product we deliver. Commitment to Quality and Innovation:We continuously strive to enhance our products in terms of quality, stability, and reproducibility, aligning with customer needs and regulatory expectations. Our goal is to provide affordable and reliable products\u00a0without compromising on excellence. Strong Regulatory and Technical Support:\u00a0Our experienced Regulatory Affairs Team\u00a0provides comprehensive support to customers worldwide. The team is well-versed with the requirements of various global regulatory agencies, ensuring smooth documentation and compliance. Long-Term Business Relationships:\u00a0We believe in nurturing long-term partnerships\u00a0with our customers and associates. Our strong global network reflects this trust \u2014 exports account for nearly 90%\u00a0of our total turnover. Sustainable and Safe Practices:\u00a0We focus on developing reproducible, efficient, and hazard-free processes, ensuring a safe and sustainable work environment. We are equally committed to environmental protection\u00a0and contributing positively to the community. Skilled and Dedicated Team:\u00a0Our success is driven by our highly qualified and experienced team, who ensure quality and compliance at every stage of production. R&D Excellence:\u00a0Our R&D department\u00a0synthesizes and characterizes various impurity standards, which we supply to our customers worldwide. Continuous innovation and scientific expertise are at the core of our operations. Milestones Company\u2019s significant milestones since inception. Year Milestones 2024 Audited and approved by ANVISA authorities CBPF\/GMP certificate received for Trimetazidine Dihydrochloride and Dexchlorpheniramine maleate 2013 & 2017 Audited and approved by EU authorities. EU-GMP Certificate received for Trimetazidine Dihydrochloride. 2011 US FDA has inspected and classified our manufacturing facility as acceptable as per USFDA regulatory requirements. 2009 Audited and approved by Korean FDA (MFDA). 2008 Maharashtra State Export Award 2004 Became a WHO-GMP certified company. 1989-90 Export Award and Certificate of Merit from Chemixcil. 1987 M.L. Dahanukar Enterpreneurship Award. 1985 Raigad District Award. 1981 R&D department is recognized by Department of Scientific and Industrial Research (DSIR),\u00a0 Government of India\u00a0 1979 Republic Day National Award for Import Substitute -Vitamin B2-5 Phosphate Sodium 1979 Anek Prayog Pvt Ltd was founded 1972 Introduced Vitamin B2-5 Phosphate Sodium, for the first time in India. 1972 Nivedita Chemicals Pvt. Ltd founded. Mission ● To manufacture vital drugs as import substitutes, so that we can become a self-sufficient nation in the realm of medicine and healthcare. ●To ensure customer satisfaction on quality and timely delivery of our products, as per the regulatory and quality standards followed internationally. ● To provide a safe working environment through effective work practices, staff training, enhancement of infrastructure, and the use of state-of-the-art technology. ● To meet dynamically changing, diverse consumer needs through supply and marketing of quality products and services. ● To be engaged in continuous Research and Development activities in order to foster innovation in the pharmaceutical industry. ● To develop processes and policies that reflect our corporate social responsibility. ● We are committed to continual quality improvement that emphasizes the accountability of every employee for product quality, workplace excellence, and the overall growth of our business. Vision To be a preferred healthcare partner for pharmaceutical industries in India, and globally.<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"blank-template.php","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"class_list":["post-3402","page","type-page","status-publish","hentry"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/relstate.esy.es\/bmw\/wp-json\/wp\/v2\/pages\/3402","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/relstate.esy.es\/bmw\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/relstate.esy.es\/bmw\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/relstate.esy.es\/bmw\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/relstate.esy.es\/bmw\/wp-json\/wp\/v2\/comments?post=3402"}],"version-history":[{"count":281,"href":"https:\/\/relstate.esy.es\/bmw\/wp-json\/wp\/v2\/pages\/3402\/revisions"}],"predecessor-version":[{"id":7178,"href":"https:\/\/relstate.esy.es\/bmw\/wp-json\/wp\/v2\/pages\/3402\/revisions\/7178"}],"wp:attachment":[{"href":"https:\/\/relstate.esy.es\/bmw\/wp-json\/wp\/v2\/media?parent=3402"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}