Around 80% of the global population incorporates medicinal products made from herbs. Herbs play a major role in conventional medicine and are also frequently employed in naturopathic, homeopathic, ayurveda, and other healthcare practices. The herbal products are vulnerable to intrusion from numerous paths, degradation, and changes in their chemical structure because they are predominantly organic (plant-based). Hence, it is crucial to establish and implement quality control criteria for medicinal products made from herbs to guarantee both their safety and effectiveness. There are numerous factors in standardization alone, including gross morphology, microscopy, physical characteristics, and chemical, chromatographic, and spectroscopic fingerprinting. Standardization of herbal medications increases their security and therapeutic efficacy while potentially gaining global popularity. Because herbal remedies are derived from natural sources, adverse reactions, counterfeiting, and tampering are less likely. From this review, the concept of standardization of herbal drugs, as well as their classification, advantages, and limitations, is described. It also includes the need and scope for standardization of herbal drugs, its standardization method, and pharmacopeial standards.