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Your premier destination for comprehensive consultancy services tailored to meet your regulatory needs. With a specialization in FDA registrations, IPO trademarks, BOC accreditation, PCAB compliance, and a myriad of other regulatory requirements, we offer expert guidance and support to navigate the complexities of today's regulatory landscape.

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FDA Registration

Specializes in guiding companies through the intricate process of FDA registration, ensuring compliance with regulatory standards and facilitating market access.

IPO Trademark Registration

Your gateway to seamless IPO trademark registration. Trust our experts to safeguard your brand's identity

BOC Import/export Accreditation

Your solution for seamless BOC importation and exportation accreditation. Navigate international trade regulations with confidence

PCAB

Trust Pharmacopoeia Consultancy to guide you through every step of the PCAB registration process, empowering your business to thrive in the competitive marketplace. Let us be your strategic ally on the path to success

BAI Registration

We streamline the registration process with the Bureau of Animal Industry (BAI), ensuring your products meet all necessary requirements for market entry

Website Development Services

We create customized websites tailored to elevate your online presence and drive success. Trust Pharmacopoeia Consultancy to bring your digital vision to life and propel your business forward in the digital age

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Navigate complex regulatory landscapes, streamline processes, and achieve compliance with confidence

  • FDA Registration
  • IPO Registration
  • BOC import/export accreditation
  • DTI Registration
  • PCAB
  • BAI registration
  • GMP certification and compliance
  • Website Development
  • Halal Certification
  • Document, Plan, Procedure formulation
  • BIR, Bookkeeping, Accounting
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Shape PHARMACOPOEIA CONSULTANCY

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We provide tailored solutions to meet your regulatory and business needs. Partner with Pharmacopoeia Consultancy and unlock the potential for success in the pharmaceutical industry. Contact us today to learn more about how we can support your goals

  • FDA Registration
  • IPO Registration
  • BOC Accreditation
  • PCAB
  • BAI registration
  • GMP Certification and Compliance
  • Halal Certification
  • Procedure, Plan, document Formulation
  • Website Development
  • BIR, Bookkeeping, Accounting
  • DTI Registration
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STEP 1
Review and Collect All Necessary Documents

Ensure that you collect and review all necessary documents, including both legal and technical papers. This thorough preparation is essential for a smooth and compliant process.

STEP 2
Click "Apply Now"

Complete the online application form.

STEP 3
Upload all the documents and wait for approval

Once you've uploaded all the necessary documents, one of our consultants will reach out to you. 

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Get your FDA License to Operate in as Fast

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Let Pharmacopoeia Consultancy take the reins of your establishment registration process with regulatory agencies such as the FDA, BAI, and more.

  • Distributor (Importer, exporter, wholesaler)
  • Trader
  • Manufacturer
  • Drugstore
  • Retailer
  • retail outlets for non-prescription drugs (RONPDS)
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Register your Product in as fast as

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Our expert team specializes in navigating the intricate requirements of these regulatory bodies such as FDA, BAI, IPO, and more. Ensuring a smooth and efficient registration process for your products.

  • Cosmetic Product Notification (FDA)
  • Medical Device Registration (CMDN/CMDR)
  • Food Product (CPR)
  • Drug/Pharmaceutical Product (CPR)
  • Household/Urban Hazardous Products
  • Food Supplement (CPR)
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January 9, 2025

Why Pharmacopoeia Is For Your Business

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January 9, 2025

How Manufacturer Secured Their FDA LTO Approval In

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LTO is an authorization issued by the FDA to an establishment to grant permission to undertake a trade or carry out a business activity, such as manufacturing, importation, exportation, sale, offering for sale, distribution, or transfer of products.

Initial LTO has a validity of 1 to 2 years, while renewal is valid for 5 years.

The LTO shall be renewed within 90 days before its expiration as per Administrative Order 2020-017.

you may send us a message or email us at [email protected] and one of our consultant will answer all your queries.

you may send us a message or email us at [email protected] and one of our consultant will answer all your queries.

Unless the LTO is revoked, validity of GMP Certificate shall be coterminous with the LTO validity, whereas the HACCP Certificate shall only be valid for one (1) year.

you may send us a message or email us at [email protected] and one of our consultant will answer all your queries.

All pharmaceutical products, medical device, cosmetics, Household, vapor products, processed food and food products including food additives, food supplements and bottled water manufactured and/or distributed (i.e. imported, exported and/or wholesale for local distribution), for trade and/or repacked are required to secure a Certificate of Product Registration before these are sold, offered for sale or use, distributed or supplied, among other marketing and promotional activities .

No. Any change from the initially approved application, except for changes equivalent to initial application, shall be filed as amendment (e.g. compliance to CPR remarks, and other post-approval changes as per FDA Circular No. 2020-033) prior to filing of renewal application.

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Specialized in FDA registrations, IPO trademarks, BOC accreditation, PCAB compliance, and a myriad of other regulatory requirements, we offer expert guidance and support to navigate the complexities of today's regulatory landscape.

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  • address: Brgy. Sto Cristo, San Jose Del Monte, Bulacan
  • email: [email protected]
  • phone: 0938-550-4272
  • work time: mon-sat: 08.00 - 06:00
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